HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461706Generated: October 29, 2026
Hydrochloric Acid → HCID 12232943, compound
https://huagongshe.com/reaction/461706
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 12232929 | HCID 12232929 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 12232943 | HCID 12232943 | — |
Reaction Steps
A mixture of 15.5 parts of diethyl 2-methyl-2-[p-(5-methyl-2-thenoyl)phenyl]malonate and 120 parts of sodium hydroxide solution 5% is stirred and refluxed for 5 hours. The reaction mixture is cooled and shaken twice with 80 parts of benzene. The aqueous phase is acidified with concentrated hydrochloric acid solution. After standing for 10 minutes, the product is extracted with chloroform. The extract is washed with water, dried, filtered and evaporated. The residue is triturated in pertroleumether. The crude product is filtered off and purified by column-chromatography using a mixture of chloroform and 10% of methanol. The pure fractions are collected and the solvent is evaporated. The residue is crystallized from acetonitrile at -20 ° C, yielding p-(5-methyl-2-thenoyl)hydratropic acid; mp. 93.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04064132 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-93fb3baf8b5d488e87a3009dd89557ef |
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| Source note | uspto-grants-1977_12 |
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