HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461739Generated: October 29, 2026
Ethanol → 2-Methyl-3-(2-thenoyl)hydratropic acid
https://huagongshe.com/reaction/461739
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Methyl-3-(2-thenoyl)hydratroponitrile | HCID 21391787 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-3-(2-thenoyl)hydratropic acid | HCID 21391751 | — |
Reaction Steps
A mixture of 6 parts of 2-methyl-3-(2-thenoyl)hydratroponitrile, 2.7 parts of potassium hydroxide, 28 parts of ethanol and 3.5 parts of water is stirred and refluxed for 44 hours. The reaction mixture is evaporated. The residue is taken up in water and washed twice with 80 parts of water. The aqueous phase is acidified with concentrated hdrochloric acid solution. The separated oily product is extracted with ether. Then the latter is dried and evaporated. The oily residue solidifies on triturating in petroleumether. The product is crystallized from acetonitrile at -20° C, yielding a first fraction of 2-methyl-3-(2-thenoyl)hydratropic acid; mp. 118.7° C. The mother-liquor is evaporated. The residue solidifies on triturating in petroleumether, yielding a second fraction of 2-methyl-3-(2-thenoyl)hydratropic acid; mp. 100° 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-05c59b9d97b242469c7f1922e7bb86f6 |
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| Source note | uspto-grants-1977_12 |
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