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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762298Generated: October 25, 2026

Potassium Carbonate → (N-Methyl-3-Trifluoromethylbenzylsulfonamido)Acetonitrile

https://huagongshe.com/reaction/1762298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantAcetonitrile, 2-(methylamino)-HCID 36652—
Reactant3-(Trifluoromethyl)phenylmethanesulfonyl chlorideHCID 2794646—
SolventWaterHCID 962—
Product(N-Methyl-3-Trifluoromethylbenzylsulfonamido)AcetonitrileHCID 15615993—

Reaction Conditions

Temperature70 °C

Reaction Steps

In this example 36.1 g of 3-trifluoromethylbenzylsulfonyl chloride was added cautiously to a solution containing 29.8 g of the hydrochloride salt of methylaminoacetonitrile and 38.7 g of potassium carbonate in 130 ml of water at room temperature. The reaction mixture was maintained at about 70° C. for about four hours. The mixture was allowed to cool and then extracted with ethyl ether. The ethyl ether extract was dried over magnesium sulfate and evaporated to dryness. The residue was vacuum filtered through silica gel using 3% vol. tetrahydrofuran: chloroform as eluent. 29 g of the title compound was obtained as a waxy white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831179
Source datasetuspto-grants-1989_05
ORD IDord-75d1dcd69b9e4abab9a3ac4316916b70
Source noteuspto-grants-1989_05