HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120870Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 10262220, compound
https://huagongshe.com/reaction/2120870
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 23435638 | HCID 23435638 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 10262220 | HCID 10262220 | 94% |
Reaction Steps
To a dichloromethane solution of oxalyl chloride was added DMSO at −78° C., the mixture was stirred at −78° C. for 15 min and followed by addition of a dichloromethane solution of compound the above Compound 26. The reaction mixture was stirred for 30 min at −78° C., then triethylamine was added, after which the reaction mixture was allowed to warm to room temperature gradually. To the reaction mixture was added ethyl acetate and brine. The organic phase was dried over magnesium sulfate, and the solvent was removed under reduced pressure. The crude product, obtained in 94% yield, was used directly for the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06693108B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-cb5c81f3b0724a52b32367de62573274 |
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| Source note | uspto-grants-2004_02 |
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