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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830992Generated: October 25, 2026

2-Nitrobenzoyl chloride → N-[4-bromo-3-(trifluoromethyl)phenyl]-2-nitrobenzamide

https://huagongshe.com/reaction/1830992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Nitrobenzoyl chlorideHCID 11875—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromo-3-(trifluoromethyl)anilineHCID 67852—
SolventEthyl AcetateHCID 8857—
ProductN-[4-bromo-3-(trifluoromethyl)phenyl]-2-nitrobenzamideHCID 1300995—

Reaction Steps

A solution of 3-amino-6-bromobenzotrifluoride (Fluka, Buchs, Switzerland; 24.0 g, 100 mmol) in EtOAc (240 mL) is added to a stirred aqueous solution of sodium hydroxide (110 mL of 1 M) at room temperature. This stirred solution is then treated dropwise over 30 minutes with a solution of 2-nitrobenzoyl chloride (Fluka, Buchs, Switzerland; 14.5 mL, 110 mmol) in EtOAc (150 mL). The resulting mixture is then stirred for 30 min at ambient temperature. The mixture is extracted with EtOAc (3×100 mL) and the combined extracts are sequentially washed with hydrochloric acid (2×100 mL of 2M), water (2×100 mL), saturated aqueous sodium hydrogen carbonate solution (2×100 mL) and saturated aqueous sodium chloride (1×100 mL), dried (MgSO4), filtered and the solvent is evaporated under reduced pressure to yield the crude product which is purified by recrystallisation from EtOAc-hexane to give the title compound as a beige crystalline solid, m.p. 157–158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067543B2
Source datasetuspto-grants-2006_06
ORD IDord-fc201deeec7d410ea7b4430c763c67dc
Source noteuspto-grants-2006_06