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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898960Generated: October 28, 2026

Methylamine → 3-bromo-N-methylbenzene-1-sulfonamide

https://huagongshe.com/reaction/898960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactantm-Bromobenzenesulphonyl chlorideHCID 17943—
SolventTetrahydrofuranHCID 8028—
Product3-bromo-N-methylbenzene-1-sulfonamideHCID 7213265100%

Reaction Steps

To a solution of 3-bromobenzenesulfonyl chloride (2.5 g, 11.2 mmol) in THF (15 mL) at 0° C. was added methylamine (2.0 M in THF; 28 mL, 56 mmol). The resulting solution was allowed to warm to room temp. and was stirred at room temp. overnight. The resulting mixture was separated between EtOAc (25 mL) and a 1 M HCl solution (25 mL). The aqueous phase was back-extracted with EtOAc (2×25 mL). The combined organic phases were sequentially washed with water (2×25 mL) and a saturated NaCl solution (25 mL), dried (MgSO4) and concentrated under reduced pressure to give N-methyl-3-bromobenzenesulfonamide as a white solid (2.8 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351834B1
Source datasetuspto-grants-2008_04
ORD IDord-616a00d93f32442d97dce8a5ddde3d87
Source noteuspto-grants-2008_04