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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309598Generated: November 2, 2026

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

https://huagongshe.com/reaction/2309598

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 folllowed 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 numberUS04695654
Source datasetuspto-grants-1987_09
ORD IDord-77aae6a0dbbe425cb0b2cfa2b1230cee
Source noteuspto-grants-1987_09