Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786354Generated: November 3, 2026

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

https://huagongshe.com/reaction/1786354

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 500 mL of CH2Cl2, DIEA (6.6 g) was added to the mixture, followed by DMAP (100 mg). 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, 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 N-(2-bromo-5-nitrophenyl)acetamide as a white solid. MS: 258 (M−1). Calc'd. for C8H7BrN2O3—259.06.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507748B2
Source datasetuspto-grants-2009_03
ORD IDord-c8df9a89d8fd48619c9046359a2faaee
Source noteuspto-grants-2009_03