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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium MethoxideHCID 10942334—
ReactantEthyl 3-methoxy-3-sulfanylidenepropanoateHCID 21317901—
SolventMethanolHCID 887—
Product3-Hydroxy-5-methoxythiophene-2-carbonitrileHCID 2131791054.2%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04155996
Source datasetuspto-grants-1979_05
ORD IDord-674dc42c9aa846ea911fcc3cd67a7335
Source noteuspto-grants-1979_05