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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921870Generated: October 30, 2026

Bromoacetyl bromide → 2-bromo-N-(2-chloro-5-cyano-3-nitrophenyl)acetamide

https://huagongshe.com/reaction/921870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
Reactant3-Amino-4-chloro-5-nitrobenzonitrileHCID 71755999—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product2-bromo-N-(2-chloro-5-cyano-3-nitrophenyl)acetamideHCID 8992234182.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of 3-amino-4-chloro-5-nitrobenzonitrile (300 mg, 1.518 mmol) in DCM (12 mL) at 0° C. was added TEA (0.635 mL, 4.56 mmol) and then 2-bromoacetyl bromide (0.291 mL, 3.34 mmol) was added drop wise. The reaction mixture was stirred at 0° C. for 1 h. LC-MS indicated a new peak. Then it was diluted with DCM and saturated aqueous sodium bicarbonate solution was added. After separating the layers, the aqueous layer was further extracted with DCM. The combined organic extracts were washed with water, brine, dried over MgSO4, filtered and concentrated. Purification via flash chromatography (0-70% EtOAc in DCM, 40 g) gave 2-bromo-N-(2-chloro-5-cyano-3-nitrophenyl)acetamide (400 mg) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273057B2
Source datasetuspto-grants-2016_03
ORD IDord-15d7fda8e4554376b6d878bf2682ebd2
Source noteuspto-grants-2016_03