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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375499Generated: October 29, 2026

Phenylacetyl chloride → HCID 67745344, compound

https://huagongshe.com/reaction/375499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantTriethylamineHCID 8471—
ReactantHCID 67745321HCID 67745321—
SolventDichloromethaneHCID 6344—
ProductHCID 67745344HCID 67745344—

Reaction Conditions

Temperature0 °C

Reaction Steps

0.35 cm3 of triethylamine and a solution of 0.17 cm3 of phenylacetyl chloride in 5 cm3 of dichloromethane are added to a suspension, cooled to 0° C., of 0.46 g of (4aRS,7aRS)-4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole 1,1-dioxide hydrochloride in 10 cm3 of dichloromethane. After stirring for 1 hour at 0° C. and then 1 hour at 20° C., the reaction mixture is diluted with 10 cm3 of dichloromethane, washed twice with 30 cm3 of distilled water, dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The oil obtained is crystallized from 30 cm3 of ethyl ether, the crystals are drained and dried. 0.50 g of (4aRS,7aRS)-4,4-diphenyl-6-phenylacetylperhydrothiopyrano[2,3-c]pyrrole 1,1-dioxide is obtained in the form of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484942
Source datasetuspto-grants-1996_01
ORD IDord-5b921a9a8cf4413db855e3bccb227e8f
Source noteuspto-grants-1996_01