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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972282Generated: October 29, 2026

Sodium Hydroxide → HCID 178465676, compound

https://huagongshe.com/reaction/972282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAcetamidine monohydrochlorideHCID 67170—
ReactantEthenesulfonyl chloride, 2-phenyl-HCID 107500—
SolventAcetoneHCID 180—
ProductHCID 178465676HCID 17846567676%

Reaction Steps

A mixture of acetamidine hydrochloride (28.8 g., 0.15 mole) and 50% sodium hydroxide (12.0 g., 0.15 mole) in 150 ml. of acetone is stirred for a period of 10 min. to liberate the free base. A solution of styrylsulfonyl chloride (10.1 g., 0.05 mole) in 50 ml. of acetone is added dropwise to the mixture at a temperature of 20°-25° C. with stirring. After further stirring for 10 min., the mixture is concentrated under reduced pressure to remove acetone, the concentrate diluted with 200 ml. of water and acidified with 3N hydrochloric acid to provide a precipitate. The precipitate is collected, dissolved in chloroform and the chloroform extract dried. Evaporation of the chloroform solvent under reduced pressure provides a white solid, m.p. 130°-134° C. which is crystallized from isopropyl acetate affording 8.5 g. (76% yield) of N-(STYRYLSULFONYL)ACETAMIDINE, m.p. 134.5°-137.0° C. (corr.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04052455
Source datasetuspto-grants-1977_10
ORD IDord-bffb2da52813491d8b04641dac73d8e7
Source noteuspto-grants-1977_10