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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906070Generated: October 30, 2026

Ammonia → 3-Fluoro-4-methoxybenzamide

https://huagongshe.com/reaction/906070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactant3-Fluoro-4-methoxybenzoic acidHCID 2733401—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-Fluoro-4-methoxybenzamideHCID 1775076970.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-fluoro-4-methoxybenzoic acid (400 mg, 2.4 mmol) and triethylamine (560 μl, 3.5 mmol) in tetrahydrofuran (10 mL) cooled to 0° C. was added isobutylchloroformate (320 μl, 2.4 mmol), and the mixture was stirred at 0° C. for 1 hour. The solution was warmed to room temperature and was saturated with ammonia gas, then stirred for 15 hours at room temperature. The mixture was diluted with ethyl acetate, then washed with 20% aqueous citric acid, saturated aqueous sodium bicarbonate, and brine, then dried over anhydrous sodium sulfate. Filtration and concentration afforded 280 mg, 1.7 mmol (70%) of 3-fluoro-4-(methyloxy)benzamide. MS (EI) for C8H8FNO2: 170 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012956B2
Source datasetuspto-grants-2011_09
ORD IDord-ad1ea231cfb04512a027d38567788b5e
Source noteuspto-grants-2011_09