HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261238Generated: November 2, 2026
Semicarbazide hydrochloride → HCID 20395322, compound
https://huagongshe.com/reaction/261238
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Semicarbazide hydrochloride | HCID 11236 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Hydroxy-3,5-dimethylbenzene-1-sulfonyl chloride | HCID 15710042 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 20395322 | HCID 20395322 | — |
Reaction Steps
11 g (0.05 mol) of 3,5-dimethyl-4-hydroxybenzenesulphonic acid chloride and 6 g (0.05mol) of semicarbazide hydrochloride are first introduced into 50 ml of dimethylacetamide. 10 ml of 10 N sodium hydroxide solution are added dropwise to this white suspension over the course of 15 minutes at 40° C., whilst stirring. Since the reaction is exothermic, slight cooling must be applied. The mixture is then stirred for a further 4 hours at 40° C. After cooling to 0° C., the sodium chloride which has precipitated is filtered off and the filtrate is concentrated completely under reduced pressure. The residue is dissolved in a small amount of water and is cooled to 0°-5° C. Hereupon, 3.5-dimethyl-4-hydroxybenzenesulphonylsemicarbazide, of melting point 243° C. (with decomposition), crystallises out.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04164611 |
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| Source dataset | uspto-grants-1979_08 |
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| ORD ID | ord-2f13a7581cb14b0fa94d16ee411735a8 |
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| Source note | uspto-grants-1979_08 |
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