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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786357Generated: November 1, 2026

Acetyl chloride → N-(2-Bromo-5-nitrophenyl)acetamide

https://huagongshe.com/reaction/1786357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Bromo-5-nitroanilineHCID 82607—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(2-Bromo-5-nitrophenyl)acetamideHCID 21959509—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Bromo-5-nitroaniline (10 g) was dissolved in CH2Cl2 (500 mL), DIEA (6.6 g) was added to the mixture, followed by 100 mg of DMAP. The mixture was cooled to 0° C. in ice bath. Acetyl chloride (4 g in 50 mL CH2Cl2) was added dropwise to the reaction mixture, which was then stirred at RT over 3 h, and extracted once with saturated NaHCO3 solution and once with brine. The separated organic layer was dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel with 1:1 EtOAc:Hexane to 100% EtOAc to afford a white solid. MS: 258 (M−1). Calc'd. for C8H7BrN2O3—259.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507748B2
Source datasetuspto-grants-2009_03
ORD IDord-5dbe9bdbb2cd4473a7e80518da7d60af
Source noteuspto-grants-2009_03