Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563104Generated: October 26, 2026

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

https://huagongshe.com/reaction/563104

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 numberUS08067453B2
Source datasetuspto-grants-2011_11
ORD IDord-029d36e173d0454ea399e35c02f0556e
Source noteuspto-grants-2011_11