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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747458Generated: October 25, 2026

Methanol → Ethyl 6-(4-fluoro-1-naphthyl)-5-hydroxy-6-oxohexanoate

https://huagongshe.com/reaction/747458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium FormateHCID 2723810—
ReactantEthyl 5-bromo-6-(4-fluoro-1-naphthyl)-6-oxohexanoateHCID 18174722—
SolventEthyl AcetateHCID 8857—
ProductEthyl 6-(4-fluoro-1-naphthyl)-5-hydroxy-6-oxohexanoateHCID 18174704—

Reaction Steps

A mixture of ethyl 5-bromo-6-(4-fluoro-1-naphthyl)-6-oxohexanoate (34.3 g), sodium formate (34.0 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-(4-fluoro-1-naphthyl)-5-hydroxy-6-oxohexanoate was obtained as a yellow oil (19.0 g, 65%) from an ethyl acetate-hexane (1:4, v/v)-eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396848B1
Source datasetuspto-grants-2008_07
ORD IDord-1e793f0b562b41f9afba3943552c21d5
Source noteuspto-grants-2008_07