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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267583Generated: October 31, 2026

Triethylamine → 3-[4-(2,4,6-Trimethylbenzenesulfonamido)benzenesulfonyl]acrylonitrile

https://huagongshe.com/reaction/267583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Mesitylenesulfonyl chlorideHCID 13046—
Reactant2-Cyanovinyl 4-aminophenyl sulfoneHCID 54561326—
SolventChloroformHCID 6212—
Product3-[4-(2,4,6-Trimethylbenzenesulfonamido)benzenesulfonyl]acrylonitrileHCID 54042124—

Reaction Steps

A solution of 6.6 g (0.03 mol) of 2,4,6-trimethylbenzenesulfonyl chloride in 50 ml chloroform is added at room temperature to a stirred slurry of 6.3 g (0.03 mol) of 3-(4-aminobenzenesulfonyl)acrylonitrile in 100 ml chloroform, the slurry additionally containing 4 ml (0.03 mol) triethylamine, portionwise over a five minute period. After 3 hours stirring the reaction mixture is filtered. The chloroform solution is thereafter washed with water, dilute hydrochloric acid, and water, in that order, separated from the water layer, dried over anhydrous magnesium sulfate and evaporated. The recovered 3-[4-(2,4,6-trimethylbenzenesulfonamido)benzenesulfonyl]acrylonitrile has the formula: ##SPC18##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03943154
Source datasetuspto-grants-1976_03
ORD IDord-501b42157c7c48e993889e85ba5b34ea
Source noteuspto-grants-1976_03