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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432044Generated: October 31, 2026

Ammonia → 1-(4-Fluorophenyl)-3-oxo-1,3-dihydro-2-benzofuran-5-carboxamide

https://huagongshe.com/reaction/432044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1-(4-Fluorophenyl)-1,3-dihydro-3-oxo-5-isobenzofurancarboxylic acidHCID 9943399—
SolventTolueneHCID 1140—
SolventThionyl ChlorideHCID 24386—
Product1-(4-Fluorophenyl)-3-oxo-1,3-dihydro-2-benzofuran-5-carboxamideHCID 4678161880%

Reaction Steps

A stirred suspension of 1-(4-fluoro-phenyl)-3-oxo-1,3-dihydro-isobenzofuran-5-carboxylic acid (1 g, 3.7 mmol) in thionyl chloride (25 mL) was heated at reflux for 25 min, during which time the solid dissolved. The thionyl chloride was then evaporated, and the residue was dissolved in toluene, and again evaporated. The residue was dissolved in toluene (15 mL) and was treated with a solution of ammonia in ether and a heavy precipitate formed. The mixture was stirred overnight, diluted with toluene and aqueous ammonia solution, and filtered. The residue was dried to give the title compound as a white solid (0.80 g, 80%). 1H NMR (d6-DMSO): δ 6.81 (s, 1H), 7.25 (t, 2H), 7.40 (dd, 2H), 7.54 (d, 1H), 7.59 (bs, 1H), 8.24 (bs, 1H), 8.24 (dd, 1H), 8.42 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660873B2
Source datasetuspto-grants-2003_12
ORD IDord-6906c31edb3e4dc8810e57e767090f6e
Source noteuspto-grants-2003_12