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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563109Generated: October 25, 2026

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

https://huagongshe.com/reaction/563109

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 numberUS08067453B2
Source datasetuspto-grants-2011_11
ORD IDord-97a37b0a8dfa46f98ae5fbe2570892a2
Source noteuspto-grants-2011_11