Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096350Generated: November 2, 2026

3-Fluoro-N-methoxy-N-methylbenzamide → 3-Fluoroacetophenone

https://huagongshe.com/reaction/1096350

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-N-methoxy-N-methylbenzamideHCID 21265757—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product3-FluoroacetophenoneHCID 996780.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 3-fluoro-N-methoxy-N-methylbenzamide (16 g, 87.4 mmol) in THF (150 mL) was cooled to −78° C. Vinylmagnesium bromide (120 mL, 120 mmol) was added slowly. The mixture was stirred at −78° C. for 10 min, at rt for 3 h, and quenched by addition of 1 N aq HCl (100 mL) at 0° C. The aqueous layer was extracted with EtOAc (100 mL). The combined organic phase was washed with brine (50 mL), dried over Na2SO4, and concentrated. The residue was purified by column chromatography to afford 1-(3-fluorophenyl)ethanone (9.7 g, yield: 75%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138178B2
Source datasetuspto-grants-2012_03
ORD IDord-8ac32a86dd7a4993afc8b7222b47a66e
Source noteuspto-grants-2012_03