HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983647Generated: November 1, 2026
Dimethyl Sulfoxide → HCID 22561004, compound
https://huagongshe.com/reaction/983647
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 131724779 | HCID 131724779 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22561004 | HCID 22561004 | — |
Reaction Steps
At −60° C., a solution of 49.37 mg (0.63 mmol) of dimethyl sulfoxide (DMSO) in 0.5 ml of dichloromethane was added dropwise to a solution of 40.10 mg (0.32 mmol) of oxalyl chloride in 2 ml of dichloromethane. The mixture was stirred at −60° C. for 15 min, and a solution of 58.00 mg (0.21 mmol) of methyl &(2-cyanobenzyl)-7-hydroxyheptanoate from Ex. XXIIId in 1 ml of dichloromethane was then added dropwise. The mixture was stirred at −60° C. for another 15 min, 106.58 mg (1.05 mmol) of triethylamine were added, the cooling bath was removed and the mixture was stirred for 2 h. Water was added, the mixture was extracted with dichloromethane, the combined organic phases were dried over Na2SO4, the solvent was removed and the crude product was dried under high vacuum. The resulting aldehyde could be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06864287B1 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-b3003e9544fc4d61b7f9e485ce8d795c |
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| Source note | uspto-grants-2005_03 |
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