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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339834Generated: October 30, 2026

2,4-Dimethoxybenzylamine → C-(3-Bromophenyl)-N-(2,4-dimethoxybenzyl)methanesulfonamide

https://huagongshe.com/reaction/339834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DimethoxybenzylamineHCID 597250—
Reactant(3-bromophenyl)methanesulfonyl ChlorideHCID 2761451—
SolventDichloromethaneHCID 6344—
ProductC-(3-Bromophenyl)-N-(2,4-dimethoxybenzyl)methanesulfonamideHCID 68292274—

Reaction Steps

While cooling with ice, 9.90 g of 3-bromobenzylsulfonyl chloride were initially charged in 120 ml of dichloromethane, and a solution of 11.55 ml of 2,4-dimethoxybenzylamine in 60 ml of dichloromethane was added dropwise within 15 minutes. The reaction mixture was allowed to come to room temperature and stirred for 1 hour. Subsequently, the mixture was washed with 50 ml of water, with 100 ml of 1 N aqueous hydrochloric acid, with 100 ml of saturated aqueous sodium hydrogencarbonate solution and finally once more with 100 ml of water. The organic phase was dried over MgSO4 and concentrated by rotary evaporation. The residue (14.30 g) was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895547B2
Source datasetuspto-grants-2014_11
ORD IDord-ea1f3e3aa0b049579333607fb37f4ba8
Source noteuspto-grants-2014_11