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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Acetonitrile, 2-(methylamino)- | HCID 36652 | — |
| Reactant | 3-(Trifluoromethyl)phenylmethanesulfonyl chloride | HCID 2794646 | — |
| Solvent | Water | HCID 962 | — |
| Product | (N-Methyl-3-Trifluoromethylbenzylsulfonamido)Acetonitrile | HCID 15615993 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04831179 |
|---|
| Source dataset | uspto-grants-1989_05 |
|---|
| ORD ID | ord-75d1dcd69b9e4abab9a3ac4316916b70 |
|---|
| Source note | uspto-grants-1989_05 |
|---|