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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188199Generated: October 29, 2026

4-(3-Fluorophenyl)butanoic acid → 6-Fluoro-1,2,3,4-tetrahydronaphthalen-1-one

https://huagongshe.com/reaction/2188199

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Fluorophenyl)butanoic acidHCID 14915113—
SolventWaterHCID 962—
Product6-Fluoro-1,2,3,4-tetrahydronaphthalen-1-oneHCID 1491511670.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4-(3-fluorophenyl)butanoic acid (10 g) and polyphosphoric acid (100 g) was heated to 70° C. with stirring for 2 h. The reaction mixture was cooled and water was carefully added (400 cm3). The aqueous mixture was extracted with diethyl ether (3×75 cm3) and the combined extracts were washed sequentially with aqueous potassium hydroxide solution (1 M, 75 cm3), water (75 cm3) and saturated aqueous sodium chloride solution (75 cm3). The combined organic extracts were dried (Na2SO4), and the solvent was distilled off under reduced pressure. The crude product (6.58 g) was purified by column chromatography [silica, eluting with petroleum ether (b. p. 40-60° C.)-ethyl acetate (20:1)] to afford the title compound (6.36 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410592B1
Source datasetuspto-grants-2002_06
ORD IDord-19cf1e972378486cb04c825309e9e77a
Source noteuspto-grants-2002_06