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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395663Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/395663

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktSodium FormateHCID 2723810—
EduktEthyl 5-bromo-6-(4-fluoro-1-naphthyl)-6-oxohexanoateHCID 18174722—
LösungsmittelEthyl AcetateHCID 8857—
ProduktEthyl 6-(4-fluoro-1-naphthyl)-5-hydroxy-6-oxohexanoateHCID 18174704—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605629B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-efb4936ba28c428d8cd2e3ca784b8740
Quellennotizuspto-grants-2003_08