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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805942Generated: October 31, 2026

Benzoyl chloride → 2(S)-(benzoyloxymethyl)-1,3-oxathiolane

https://huagongshe.com/reaction/1805942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantHCID 46244897HCID 46244897—
SolventDichloromethaneHCID 6344—
Product2(S)-(benzoyloxymethyl)-1,3-oxathiolaneHCID 5960899144.6%

Reaction Steps

2(S)-(Hydroxymethyl)-1,3-oxathiolane (0.25 mmol, 30 mg, 1.0 equiv.) recovered from Example 3 was treated with benzoyl chloride (0.25 mmol, 35 mg, 1.0 equiv.), triethylamine (0.25 mmol, 25 mg, 1.0 equiv.) in dichloromethane (1 mL) at ambient temperature while monitoring the reaction progress by TLC. After 1 h, the reaction was extracted with saturated ammonium chloride solution and brine. The organic phase was concentrated and chromatographed on silica gel to give 2(S)-(benzoyloxymethyl)-1,3-oxathiolane (25 mg, 44.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354546B2
Source datasetuspto-grants-2013_01
ORD IDord-64a39b8ecdad4030abc99a3fd9619842
Source noteuspto-grants-2013_01