HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128408Generated: October 25, 2026
Sodium Hydroxide → HCID 178465676, compound
https://huagongshe.com/reaction/128408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | Ethenesulfonyl chloride, 2-phenyl- | HCID 107500 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178465676 | HCID 178465676 | 76% |
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 3 N 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04259482 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-87102362e1fd4358a8c99927fc0420cb |
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| Source note | uspto-grants-1981_03 |
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