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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006813Generated: October 28, 2026

Pyridine → HCID 86584850, compound

https://huagongshe.com/reaction/1006813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 86584851HCID 86584851—
SolventDichloromethaneHCID 6344—
ProductHCID 86584850HCID 8658485023.8%

Reaction Steps

To a solution of (2S,4R)-(4-mercapto-1-methanesulfonyl-pyrrolidin-2-yl)-methanol (0.28 g) in dichloromethane (10 ml) were added pyridine (0.131 g) and acetic anhydride (0.160 g). The reaction mixture was stirred for 4 h at room temperature, treated with ice/water and extracted with EtOAc. The organic phase was washed with a saturated solution of sodium bicarbonate and brine, dried over magnesium sulphate and concentrated. The residue was chromatographed on silica gel using EtOAc/hexane 1:2 as eluent to obtain thioacetic acid (3R,5S)-S-(5-hydroxymethyl-1-methanesulfonyl-pyrrolidin-3-yl) ester (0.080 g) as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790860B2
Source datasetuspto-grants-2004_09
ORD IDord-1ef822e4a9e9483a8cb119c7fcf4a99e
Source noteuspto-grants-2004_09