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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232172Generated: October 28, 2026

Triethylamine → N-(4-benzyloxy-2,2-difluorobutyl)-p-toluenesulfonamide

https://huagongshe.com/reaction/232172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
Reactant4-Benzyloxy-2,2-difluorobutylamineHCID 19860694—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductN-(4-benzyloxy-2,2-difluorobutyl)-p-toluenesulfonamideHCID 19860703—

Reaction Steps

To a solution of 4-benzyloxy-2,2-difluorobutylamine (5.16 g, 20.5 mM) and triethylamine (4.4 g, 43.4 mM) in dry dichloromethane is added toluenesulfonyl chloride (4.14 g, 21.7 moles). The mixture is stirred at room temperature overnight. Additional dichloromethane is added, and the organic phase is washed with 1N HCl followed by a water wash. Drying (Na2SO4) and evaporation of the solvent yields a white solid which is dissolved in a small volume of ether. Addition of petroleum ether yields the compound, N-(4-benzyloxy-2,2-difluorobutyl)-p-toluenesulfonamide as white crystals: 7.0 g (92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851448
Source datasetuspto-grants-1989_07
ORD IDord-64df84c481fa46cc918bc8e091d7c46b
Source noteuspto-grants-1989_07