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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395653Generated: October 26, 2026

Methanol → Ethyl 6-(5-chloro-2-thienyl)-5-hydroxy-6-oxohexanoate

https://huagongshe.com/reaction/395653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium FormateHCID 2723810—
ReactantEthyl 5-bromo-6-(5-chloro-2-thienyl)-6-oxohexanoateHCID 18174681—
SolventEthyl AcetateHCID 8857—
ProductEthyl 6-(5-chloro-2-thienyl)-5-hydroxy-6-oxohexanoateHCID 18174715—

Reaction Steps

A mixture of ethyl 5-bromo-6-(5-chloro-2-thienyl)-6-oxohexanoate (64.4 g), sodium formate (60.0 g) and methanol (150 ml) was stirred with heating under reflux for 16 hours. The reaction mixture was diluted with ethyl acetate (500 ml) and washed with water (200 ml×2). The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography, and ethyl 6-(5-chloro-2-thienyl)-5-hydroxy-6-oxohexanoate was obtained as a yellow oil (21.6 g, 41%) from an ethyl acetate-hexane (1:4, v/v)-eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605629B1
Source datasetuspto-grants-2003_08
ORD IDord-dd0907b18aad4b3b8bd8621388d93a03
Source noteuspto-grants-2003_08