HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358371Generated: October 29, 2026
Dimethyl Sulfoxide → HCID 20448834, compound
https://huagongshe.com/reaction/358371
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 22827437 | HCID 22827437 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20448834 | HCID 20448834 | 61% |
Reaction Steps
Oxalyl chloride (48 microliters; 0.55 mmole) was dissolved in 2 ml of dry dichloromethane, and the solution was cooled to -30° C. Dimethyl sulfoxide (78 microliters; 110 mmoles) was added, and the mixture was stirred for 3 minutes. A solution of 158 mg (0.5 mmole) of 4(R)-t-butyldimethylsilyloxy-2-(4-hydroxybutylthio)-2-cyclopentenone in 1 ml of dry dichloromethane was added over the course of 1 minute, and the mixture was stirred at -30° C. for 30 minutes. Then, 5 ml of a saturated aqueous solution of ammonium chloride was added, and the mixture was extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, filtered, and concentrated. The resulting oily product was chromatographed on a silica gel column using hexane/ethyl acetate (5/1) to give 96 mg (yield 61%) of 4(RS)-t-butyldimethylsilyloxy-2-(4-oxobutylthio)-2-cyclopentenone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04466980 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-2d1225f6b1e14b0e91046915c5171c3e |
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| Source note | uspto-grants-1984_08 |
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