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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406652Generated: October 30, 2026

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

https://huagongshe.com/reaction/406652

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 numberUS08754076B2
Source datasetuspto-grants-2014_06
ORD IDord-3658eefa86f84afdacaf7098d176c428
Source noteuspto-grants-2014_06