> ## Documentation Index
> Fetch the complete documentation index at: https://reactionrepo.com/llms.txt
> Use this file to discover all available pages before exploring further.
# Oxidation with Oxalyl chloride
> Mild Oxidation Method using Oxalyl chloride as DMSO Activator
The Swern oxidation, developed by Kanji Omura and Daniel Swern in 1978, is a method used to oxidize primary alcohols to aldehydes and secondary alcohols to ketones using activated dimethyl sulfoxide (DMSO), oxalyl chloride as a oxidizing agent, triethylamine (TEA) and dichloromethane (DCM). **1**
DMSO and Oxalyl chloride form a reactive salt (Lewis Acid) with the alcohol providing a good leaving group required for subsequent elimination.**1**
## Finding the Product for a 1° Alcohol
This section is a brief overview on how to find the product for a 1° Alcohol (Primary) using a example from a real scientific research paper.
Condensed Synthesis Overview of the Asymmetric Total Synthesis of Taxol by Mukaiyama et al. (1999)
This 61 step linear synthesis features Swern Oxidation for a total of 4 steps out of 61 steps. L-serine is the starting material and undergoes 61 steps to form Taxol.
For simplicity, this image summarizes the total steps displayed in the original paper by [Mukaiyama et al. (1999)](https://doi.org/10.1002/\(SICI\)1521-3765\(19990104\)5:1%3C121::AID-CHEM121%3E3.0.CO;2-O), showing that the synthesis of the Taxol underwent a 61 step linear synthesis. The full pathway is not shown in our example. This is to maintain clarity and focus on building towards when Swern Oxidation is used.
Retrosynthetic Analysis of Taxol
In 1999, Mukaiyama et al. published the Mukaiyama Asymmetric Total Synthesis of Taxol. Taxol, a well-known complex organic molecule, underwent retrosynthetic analysis, revealing an optically active ketone intermediate (3), which could be further simplified into a chiral aldehyde intermediate (4).
Retrosynthetic analysis is a technique in organic chemistry that breaks down complex molecules into simpler components by working backward. This method helps chemists plan a synthesis pathway by identifying key bonds to disconnect, guiding the creation of a forward-directing synthetic route.
As seen above, the chiral aldehyde intermediate (4), compound 18 undergoes a reduction via DIBAL and hexane as a solvent. Next, this reduced intermediate undergoes Swern Oxidation to form the chiral aldehyde intermediate (4).**2**
DMSO is used alongside the preferred oxidizing agent Oxalyl chloride, TEA (Triethylamine) and DCM.
If you missed the [**Background section**](/reactionrepo/docs/oxidation-reactions/swern-oxidation) on the Swern Oxidation landing page, please check it out. It's highly recommended to review the information as it covers the key characteristics the reaction and the reactants.
**Alcohol Type**
These are the 3 main types of alcohols:
* Primary
* Secondary
* Tertiary
Tertiary alcohols cannot go through Swern oxidation.
* Primary alcohols can go through Swern Oxidation to become an **Aldehyde**.
By identifying the Alcohol Type, you now know the **product** to expect.
Tracking Side Chains and Alcohol Conversion.
In Swern oxidation of primary alcohols, the process involves assigning one side chain (R) to understand the reaction better.
The colored side chain represents an R group that remains unchanged during the reaction. The alcohol group is selectively oxidized to form an aldehyde. For educational purposes, we conceptually assign the non-alcohol group as R (Side chain) to visualize the changes and reconstruct the molecule post-reaction.
The molecule isn’t taken apart during the reaction, but for understanding the process, we conceptually take it apart to visualize the changes. This allows for easy reconstruction of the molecule after oxidation, emphasizing the selective nature of the reaction for educational purposes.
**Guide to Side Chains**
1. **Assign the Side Chain (R)**: Identify the non-alcohol part of the molecule and assign it as the placeholder 'R' or side chain.
2. **Understand Its Role**: This placeholder helps track the unchanged part of the molecule, aiding in visualizing the structure before and after the reaction.
3. **Focus on the Reaction Center**: The primary alcohol is selectively oxidized to form an aldehyde. The placeholder shows how the structure is altered.
4. **Reassign the Side Chain**: After the reaction, reattach the placeholder R to the new aldehyde, demonstrating the unchanged nature of the side chain.
**Disclaimer Warning for Writing Products**
Variations on how Aldehydes may appear.
They may be differently presented in different questions as shown in the image, however they are the same structure.
Once you've identified the correct reaction and product, you can now proceed to doing the mechanism.
## Mechanism for 1° Alcohol
This section is a brief overview on how to perform the mechanism for a 1° Alcohol (Primary) using the example from above.
Resonance forms of DMSO.
DMSO is capable of undergoing resonance. This is important for the next step.
In the first step of Swern Oxidation, DMSO undergoes resonance to prepare the DMSO to perform a nucleophilic attack on Oxalyl chloride.
Nucleophillic attack using DMSO Resonance structure.
DMSO Resonance Structure performs Nucleophilic Attack, Chloride Ion acts as a Leaving Group.
In this step, the newly formed chromium-alcohol complex undergoes protonation. This protonation stabilizes the intermediate, preparing it for further rearrangement and facilitating the subsequent steps in the oxidation process.
Chlorodimethyl Sulfonium Ion Formation.
The nucleophilic attack initiates proton transfer within the Chlorosulfonium Ion to form Chlorodimethyl Sulfonium Ion its byproduct.
In this step, the Chlorosulfonium Ion decomposes after proton transfer is initiated from the chloride ion. This action releases carbon dioxide, carbon monoxide and a chloride ion.
Addition of the Primary Alcohol and 2 equivalents of TEA (Triethylamine).
This process produces a alkoxysulfonium ion intermediate. However the octet rule is violated in the newly produced ion, so TEA (Triethylamine) is needed to stabilize the molecule for further transformation.
In this step, the primary alcohol is added and SN2 substitution occurs. Chloride is a good leaving group and leaves the Chlorosulfonium Ion to produce alkoxysulfonium ion intermediate. Next, 2 equivalents of TEA (Triethylamine) is added to neutralize changes and stabilize the intermediate. This eventually forms a sulfur ylide.
Aldehyde product and DMS byproduct Formation.
Sulfur Ylide decomposes to form DMS and the desired aldehyde product.
The Sulfur ylide undergoes intramolecular elimination to cleave the ylide into the desired product and by-products.
## Finding the Product for a 2° Alcohol
This section is a brief overview on how to find the product for a 2° Alcohol (Secondary) using a example from a real scientific research paper.
Propose a Mechanism for this Reaction **3**
Oxidation of a secondary alcohol intermediate to an ketone. The groundwork to determine the product is similar to how a primary alcohol is converted.
This section is under review
This section is under review
DMSO is used alongside the preferred oxidizing agent Oxalyl chloride, TEA (Triethylamine) and DCM.
Once again if you missed the [**Background section**](/reactionrepo/docs/oxidation-reactions/swern-oxidation) on the Swern Oxidation landing page, please check it out. It's highly recommended to review the information as it covers the key characteristics the reaction and the reactants.
**Alcohol Type**
These are the 3 main types of alcohols:
* Primary
* Secondary
* Tertiary
Tertiary alcohols cannot go through Swern oxidation.
* Primary alcohols can go through Swern Oxidation to become an **Aldehyde**.
By identifying the Alcohol Type, you now know the **product** to expect.
Tracking Side Chains and Alcohol Conversion.
In Swern oxidation of primary alcohols, the process involves assigning one side chain (R) to understand the reaction better.
The colored side chain represents an R group that remains unchanged during the reaction. The alcohol group is selectively oxidized to form an aldehyde. For educational purposes, we conceptually assign the non-alcohol group as R (Side chain) to visualize the changes and reconstruct the molecule post-reaction.
The molecule isn’t taken apart during the reaction, but for understanding the process, we conceptually take it apart to visualize the changes. This allows for easy reconstruction of the molecule after oxidation, emphasizing the selective nature of the reaction for educational purposes.
**Guide to Side Chains**
1. **Assign the Side Chain (R)**: Identify the non-alcohol part of the molecule and assign it as the placeholder 'R' or side chain.
2. **Understand Its Role**: This placeholder helps track the unchanged part of the molecule, aiding in visualizing the structure before and after the reaction.
3. **Focus on the Reaction Center**: The primary alcohol is selectively oxidized to form an aldehyde. The placeholder shows how the structure is altered.
4. **Reassign the Side Chain**: After the reaction, reattach the placeholder R to the new aldehyde, demonstrating the unchanged nature of the side chain.
Once you've identified the correct reaction and product, you can now proceed to doing the mechanism.
## Mechanism for 2° Alcohol
This section is a brief overview on how to perform the mechanism for a 2° Alcohol (Secondary) using the example from above.
Resonance forms of DMSO.
DMSO is capable of undergoing resonance. This is important for the next step.
In the first step of Swern Oxidation, DMSO undergoes resonance to prepare the DMSO to perform a nucleophilic attack on Oxalyl chloride.
Nucleophillic attack using DMSO Resonance structure.
DMSO Resonance Structure performs Nucleophilic Attack, Chloride Ion acts as a Leaving Group.
In this step, the newly formed chromium-alcohol complex undergoes protonation. This protonation stabilizes the intermediate, preparing it for further rearrangement and facilitating the subsequent steps in the oxidation process.
Chlorodimethyl Sulfonium Ion Formation.
The nucleophilic attack initiates proton transfer within the Chlorosulfonium Ion to form Chlorodimethyl Sulfonium Ion its byproduct.
In this step, the Chlorosulfonium Ion decomposes after proton transfer is initiated from the chloride ion. This action releases carbon dioxide, carbon monoxide and a chloride ion.
Addition of the Secondary Alcohol and 2 equivalents of TEA (Triethylamine).
This process produces a alkoxysulfonium ion intermediate. However the octet rule is violated in the newly produced ion, so TEA (Triethylamine) is needed to stabilize the molecule for further transformation. This process is the same as the primary alcohol, except there is an additional side chain.
In this step, the secondary alcohol is added and SN2 substitution occurs. Chloride is a good leaving group and leaves the Chlorosulfonium Ion to produce alkoxysulfonium ion intermediate. Next, 2 equivalents of TEA (Triethylamine) is added to neutralize changes and stabilize the intermediate. This eventually forms a sulfur ylide.
Ketone product and DMS byproduct Formation.
Sulfur Ylide decomposes to form DMS and the desired ketone product.
The Sulfur ylide undergoes intramolecular elimination to cleave the ylide into the desired product and by-products.
## Sample Problems
Test your Knowledge.
### Question 1
Predict the Product.
This should form the expected aldehyde product as a result of oxidation of the primary alcohol on this compound.
Overall Synthesis of (+)-Pentacycloanammoxic Acid from the starting material cyclooctatetraene.
Cyclooctatetraene underwent a 15 step synthesis pathway to form the end product:(+)-Pentacycloanammoxic Acid.
For simplicity, this image summarizes total number of steps in the original paper by [Mascitti & Corey (2004)](https://doi.org/10.1021/ja044089a) to form the desired product (1). The full pathway is not shown to maintain clarity and focus on building towards when Swern oxidation is used.
The starting material, Cyclooctatetraene underwent 10 steps until it reached the formation of compound 7. Compound 7 underwent subsequent reactions, including reduction from DIBAL-H and oxidation via Swern Oxidation to form compound 8. **4**
### Question 2
Propose a Mechanism for this Reaction.
Hint: Do not confuse this with the [first example](/reactionrepo/docs/oxidation-reactions/swern-oxidation/oxidation-with-oxalyl-chloride/#finding-the-product-for-a-1-alcohol)
Tracking Side Chains and Alcohol Conversion in Swern Oxidation.
Be careful when assigning side chain placeholders. If you do not see a side chain visible that is not denoted by H or another group. Assume its a Methyl group. In the example, it was not shown, however for group tracking we have shown it in red.
When oxidizing secondary alcohols, the colored side chains represent unchanged R groups. The alcohol is selectively oxidized to form a ketone. For educational purposes, use R¹ and R² as placeholders for parts of the molecule, excluding the secondary alcohol and first side chain. This helps visualize the reaction and reconstruct the molecule post-oxidation.
The molecule isn't taken apart during the reaction, but for understanding the process, we conceptually take it apart to visualize the changes. Additionally for the sake of visual aid, we've slightly moved the yellow side chain group.
Rewrite the new Ketone product.
Condensed Synthesis Overview of the Asymmetric Total Synthesis of Taxol by Mukaiyama et al. (1999)
This 61 step linear synthesis features Swern Oxidation for a total of 4 steps out of 61 steps.
For simplicity, this image summarizes the total steps displayed in the original paper by [Mukaiyama et al. (1999)](https://doi.org/10.1002/\(SICI\)1521-3765\(19990104\)5:1%3C121::AID-CHEM121%3E3.0.CO;2-O), showing that synthesis of the Taxol underwent a 61 step linear synthesis. The full pathway is not shown in our example. This is to maintain clarity and focus on building towards when Swern Oxidation is used.
Retrosynthetic Analysis of Taxol.
The Mukaiyama Asymmetric Total Synthesis of Taxol was published in 1999 by Mukaiyama et al (1999). Taxol, a well known and difficult complex organic molecule, underwent retrosynthetic analysis. This revealed a optically active ketone intermediate (3) which could be further broken down into another basic unit (4)
Reminder: Retrosynthetic analysis is a technique in organic chemistry that breaks down complex molecules into simpler components by working backward. This method helps chemists plan a synthesis pathway by identifying key bonds to disconnect, guiding the creation of a forward-directing synthetic route.
As seen in Scheme 5 of the paper, the synthesis of an optically active ketone (3) involved a single step process using two sets of reagent combinations. First, the alkylation (Grignard reaction) of compound 22 using Methyl Magnesium Bromide (MeMgBr) This yielded an alcohol intermediate. Next, this secondary alcohol intermediate was oxidized to a ketone (3) using Swern Oxidation (Oxidation with Oxalyl chloride).**2**
## Summary
The reaction entry summary. Find the general scheme and full summarized mechanisms here.
### General Scheme
This section briefly summarizes what can and cannot undergo reactions.
* 1° Alcohols (Primary) get oxidized to **Aldehydes**.
* 2° Alcohols (Secondary) get oxidized to **Ketones**.
* 3° Alcohols (Tertiary) **do not** get oxidized at all.
### General Mechanism
This section briefly summarizes steps to find the product and perform the mechanisms.
**Quick steps to finding the product for any alcohol**
1. Identify the reagents.
2. Assign side chains (non alcohol part).
3. Selectively convert Alcohol to correct product based on alcohol type. Nothing else.
4. Keep the side chains (non alcohol part) the same and piece together the full molecule together again.
Always remember to repeatedly practice your mechanisms and getting your reagents correct. Take advantage of our materials and/or keep practicing on a whiteboard or paper until you get it right every single time.
## References
1. Omura, K.; Swern, D. Oxidation of Alcohols by “Activated” Dimethyl Sulfoxide. A Preparative, Steric and Mechanistic Study.
Tetrahedron 1978, 34 (11), 1651–1660.
DOI: 10.1016/0040-4020(78)80197-5
2. Mukaiyama, T.; Shiina, I.; Iwadare, H.; Saitoh, M.; Nishimura, T.; Ohkawa, N.; Sakoh, H.; Nishimura, K.; Tani, Y.-i.; Hasegawa, M.;
Yamada, K.; Saitoh, K. Asymmetric Total Synthesis of Taxol.
Chem. Eur. J. 1999, 5 (1), 121–161.
DOI: 10.1002/(SICI)1521-3765(19990104)5:1\<121::AID-CHEM121>3.0.CO;2-O
3. Stork, G.; Niu, D.; Fujimoto, A.; Koft, E. R.; Balkovec, J. M.; Tata, J. R.; Dake, G. R. The First Stereoselective Total Synthesis of Quinine.
J. Am. Chem. Soc. 2001, 123 (14), 3239–3242.
DOI: 10.1021/ja004325r
4. Mascitti, V.; Corey, E. J. Total Synthesis of (±)-Pentacycloanammoxic Acid.
J. Am. Chem. Soc. 2004, 126 (48), 15664–15665.
DOI: 10.1021/ja044089a
