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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689575Generated: November 2, 2026

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

https://huagongshe.com/reaction/1689575

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 numberUS08153416B2
Source datasetuspto-grants-2012_04
ORD IDord-2b1d43f87cb148e4864d59d7e1a195a5
Source noteuspto-grants-2012_04