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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883505Generated: November 2, 2026

4-Nitrobenzaldehyde → HCID 53784447, compound

https://huagongshe.com/reaction/1883505

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant3-(Trifluoromethyl)benzeneacetic acidHCID 67695—
SolventWaterHCID 962—
ProductHCID 53784447HCID 5378444780%

Reaction Steps

A solution of (3-trifluoromethyl-phenyl)-acetic acid (7.5 g, 36.7 mmol), 4-nitro-benzaldehyde (5.55 g, 36.7 mmol), triethylamine (4.8 g, 47.8 mmol), and acetic anhydride (14.3 g, 140 mmol) was refluxed for 6 hours. The reaction mixture was poured in acidified water (sulfuric acid, pH 1) and extracted with ethyl acetetate. The organic layer was evaporated and the residue was stirred with sodium bicarbonate solution. The precipitate was sucked off and the filtrate extracted with ethyl acetate. The water was acidified with hydrochloric acid and the resulting oil extracted with ethyl acetate to give 9.9 g of the desired product (80% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759420B1
Source datasetuspto-grants-2004_07
ORD IDord-b97e35ceeb7d418a94419234432bffd6
Source noteuspto-grants-2004_07