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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906374Generated: October 31, 2026

4-Nitrobenzenesulfonyl chloride → N-(Cyanomethyl)-4-nitrobenzenesulfonamide

https://huagongshe.com/reaction/1906374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzenesulfonyl chlorideHCID 7404—
ReactantSodium HydroxideHCID 14798—
ReactantAminoacetonitrile hydrochlorideHCID 11491918—
SolventWaterHCID 962—
ProductN-(Cyanomethyl)-4-nitrobenzenesulfonamideHCID 311340572.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a stirred solution of 27.8 g (0.3 moles) aminoacetonitrile hydrochloride in 200 ml water, 24 g (0.3 moles) sodium hydroxide (50% aqueous) were added. The resulting mixture was cooled to about 20° C. with an ice bath. The ice bath was removed; then 22.2 g (0.1 mole) 4-nitrobenzenesulfonyl chloride were added. The reaction mixture was stirred 18 hours at ambient temperature. The solids were filtered. The resulting wet cake was crystallized from 50 ml ethanol. The solids were dried in vacuo to give 17.5 g of the above-identified product as a dark-yellow solid, melting point 115°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04652556
Source datasetuspto-grants-1987_03
ORD IDord-b177908c9c3942a5b0e4ec6a6f7c9ae2
Source noteuspto-grants-1987_03