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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157390Generated: October 26, 2026

Bromoacetyl bromide → N-[4-(aminosulfonyl)-2-chlorophenyl]-2-bromoAcetamide

https://huagongshe.com/reaction/1157390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Amino-3-chlorobenzenesulfonamideHCID 1502014—
SolventDichloromethaneHCID 6344—
ProductN-[4-(aminosulfonyl)-2-chlorophenyl]-2-bromoAcetamideHCID 59511722—

Reaction Steps

A mixture of 750 mg (3.63 mmol) of 4-amino-3-chlorobenzenesulfonamide (A-2) and 610 mg (7.26 mmol) of sodium bicarbonate in 25 mL of CH2Cl2 was stirred at room temperature for 18 hours. Bromoacetyl bromide (A-1) was then added, and the mixture was stirred for an additional 12 hours. The mixture was then concentrated in vacuo to a yellow oil. The oil was washed with three 25 mL portions of diethyl ether, decanted, and concentrated in vacuo to give the desired product A-3 as a tan solid. MS: M+1=329.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807684B2
Source datasetuspto-grants-2010_10
ORD IDord-b0b60f6f4238438b970beae9d54a4270
Source noteuspto-grants-2010_10