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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476522Generated: October 26, 2026

Triethylamine → N-cyclopropyl-3-trifluoromethylbenzylsulfonamide

https://huagongshe.com/reaction/476522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclopropylamineHCID 69828—
Reactant3-(Trifluoromethyl)phenylmethanesulfonyl chlorideHCID 2794646—
SolventDichloromethaneHCID 6344—
ProductN-cyclopropyl-3-trifluoromethylbenzylsulfonamideHCID 1561599492.6%

Reaction Steps

In this example, 5.3 g of cyclopropylamine is mixed with 9.4 g of triethylamine and then added dropwise to a solution containing 20 g of 3-trifluoromethylbenzylsulfonyl chloride in methylene chloride at 0° C. The resulting reaction mixture is stirred at room temperature (i.e., about 20°-25° C.) for 3 hours. The reaction mixture is washed with saturated aqueous ammonium chloride and then with aqueous 1 wt.% hydrochloric acid until it was neutral. The organic layer is separated, washed twice with 50 ml of aqueous saturated sodium chloride solution, dried over magnesium sulfate and then evaporated to dryness affording 20 g of N-cyclopropyl-3-trifluoromethylbenzylsulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885027
Source datasetuspto-grants-1989_12
ORD IDord-8c78722a0a994ec08124fa80042d3719
Source noteuspto-grants-1989_12