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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212685Generated: October 31, 2026

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

https://huagongshe.com/reaction/2212685

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. After the mixture was stirred at RT over 3 h, and extracted once with saturated NaHCO3 solution and once with brine. The resulting 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 numberUS07102009B2
Source datasetuspto-grants-2006_09
ORD IDord-ee4451113d1446b3ad5a0e4fe8f27082
Source noteuspto-grants-2006_09