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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358371Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 20448834, compound

https://huagongshe.com/reaction/358371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantAmmonium ChlorideHCID 25517—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22827437HCID 22827437—
SolventDichloromethaneHCID 6344—
ProductHCID 20448834HCID 2044883461%

Reaction Conditions

Temperature-30 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04466980
Source datasetuspto-grants-1984_08
ORD IDord-2d1225f6b1e14b0e91046915c5171c3e
Source noteuspto-grants-1984_08