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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901572Generated: November 3, 2026

Bromine → 2-bromo-4-methylaminosulfonylmethyl-N-trifluoroacetylaniline

https://huagongshe.com/reaction/1901572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Methylaminosulfonylmethyl-N-trifluoroacetylanilineHCID 19970215—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-bromo-4-methylaminosulfonylmethyl-N-trifluoroacetylanilineHCID 1100329629.7%

Reaction Steps

To a chilled suspension of 4-methylaminosulfonylmethyl-N-trifluoroacetylaniline (10.9 g) in methanol (100 mL) was added sodium bicarbonate (28 g), followed by bromine (18.3 g) in methylene chloride (30 mL). The reaction mixture was then diluted with methylene chloride (70 mL) and quenched by the addition of sodium sulfite (20 g), filtered through CELITE and concentrated in vacuo to a yellow residual solid. This solid was twice reslurried in methylene chloride (300 mL) then refiltered and the filtrates evaporated in vacuo. The residual materials were combined in 10% acetone/methylene chloride solution and concentrated then purified by column chromatography (eluting with 4% acetone in methylene chloride) to give the title compound (4.10 g) mp 170° C.; TLC (methylene chloride/acetone 15:1) Rf=0.36, and the corresponding dibromide (5.56 g) TLC (methylene chloride/acetone 15:1) Rf=0.31.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578612
Source datasetuspto-grants-1996_11
ORD IDord-7fd82d0668ad417c9cbc207b049337a7
Source noteuspto-grants-1996_11