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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988628Generated: November 1, 2026

Triethylamine → 950785-37-2

https://huagongshe.com/reaction/1988628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Chloropropanesulphonyl chlorideHCID 15410—
ReactantSodium hydrideHCID 24758—
Reactant4-BromobenzylamineHCID 77571—
SolventDimethylformamideHCID 6228—
Product950785-37-2HCID 4717617194%

Reaction Steps

A solution of 4-bromobenzylamine (1.85 g, 10 mmol) and triethylamine (2 g, 20 mmol) in dimethylformamide (30 ml) was treated with 3-chloropropanesulfonyl chloride (1.78 g, 10 mmol) by dropwise addition over 10 minutes with stirring under argon. This mix was stirred for 30 minutes before being treated with a 60% suspension of sodium hydride in mineral oil (1.2 g, 30 mmol of NaH) portionwise and the whole mix stirred at room temperature for 3 days. The reaction mixture was partitioned between water (50 ml) and dichloromethane (30 ml). The organic layer was dried over sodium sulphate and reduced to minimum volume by rotary evaporation. The residue was added to a 20 g pre-packed silica column and eluted from 0-50% ethyl acetate in petroleum ether to give the title compound as a yellow oil (2.72 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642256B2
Source datasetuspto-grants-2010_01
ORD IDord-fc7c0eecd520456cacbb1ee0086daca7
Source noteuspto-grants-2010_01