HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263027Generated: November 2, 2026
Acetonitrile → 3-Hydroxy-5-methoxythiophene-2-carbonitrile
https://huagongshe.com/reaction/263027
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Ethyl 3-methoxy-3-sulfanylidenepropanoate | HCID 21317901 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Hydroxy-5-methoxythiophene-2-carbonitrile | HCID 21317910 | 54.2% |
Reaction Steps
81 g of O-methyl 2-ethoxycarbonyl-thioacetate and then 38 g of acetonitrile were added to a solution of 27 g of sodium methylate in 250 ml of methanol and the mixture was refluxed for one hour. A solution of 27 g of sodium methylate in 100 ml of methanol were added to the reaction which was cooled to 20° C. and concentrated to dryness. The residue was dissolved in water and the solution was washed with ether, acidified with concentrated hydrochloric acid and was vacuum filtered. The recovered crystals were dried to obtain 42 g of 2-cyano-3-hydroxy-5-methoxy-thiophene with a melting point of 138°-140° C. A microanalytically pure sample obtained by crystallization from isopropyl ether melted at 140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04155996 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-674dc42c9aa846ea911fcc3cd67a7335 |
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| Source note | uspto-grants-1979_05 |
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