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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1832096Generated: October 31, 2026

Dimethylamine → 4-(Bromomethyl)-N,N-dimethylbenzenesulfonamide

https://huagongshe.com/reaction/1832096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Bromomethyl)benzenesulfonyl chlorideHCID 2734409—
SolventTetrahydrofuranHCID 8028—
Product4-(Bromomethyl)-N,N-dimethylbenzenesulfonamideHCID 11044082—

Reaction Steps

4-(Bromomethyl)benzenesulfonyl chloride (5.0 g, 18.6 mmol) was dissolved in tetrahydrofuran. N,N-dimethylamine (7.7 mL, 15.5 mmol, 2M in tetrahydrofuran) and and N,N-diisopropylethylamine (3.5 mL, 20.1 mmol) were added, and the reaction was allowed to stir at ambient temperature for 2 hours. The reaction was concentrated to an oil that was partitioned between water and ethyl acetate and extracted with ethyl acetate. The organic extracts were combined, washed with brine, dried over Na2SO4, and filtered. The resulting filtrate was concentrated to an oil which deposited needles that were a mixture of the title compound and 4-chloromethyl N,N-dimethylbenzenesulfonamide. The resulting needles were collected. and dried (2.3 g, 44%). ES-MS m/z 534 (M+H) and 578 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067540B2
Source datasetuspto-grants-2006_06
ORD IDord-69a2e418d170422991ff48ea24bbf7c8
Source noteuspto-grants-2006_06