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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982014Generated: October 29, 2026

Hydrochloric Acid → 2-Methylthio-3,5-dicyano-4-hydroxythiophene

https://huagongshe.com/reaction/982014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantMethyl cyanoacetateHCID 7747—
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium HydroxideHCID 14797—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product2-Methylthio-3,5-dicyano-4-hydroxythiopheneHCID 14119770—

Reaction Steps

A cold, highly concentrated solution of 25 g of KOH in approximately 15 ml of water is slowly added dropwise to a solution of 20.0 g of cyanoacetic acid methyl ester and 18.0 g of carbon disulphide in approximately 300 ml of dimethyl formamide while stirring and cooling to below approximately 0° C. After stirring for another 20 minutes, a solution of 15.5 g of chloroacetonitrile in 10 ml of acetonitrile is added dropwise to the reaction mixture at -5° C. to 0° C. After stirring for another 30 minutes, a highly concentrated solution of 13 g of KOH in water is added and stirred for 30 minutes at 40° C. Then 29 g of methyl iodide are added dropwise and, after 30 minutes, 25 ml of concentrated hydrochloric acid. After concentration of the reaction mixture under reduced pressure to approximately 300 ml, approximately 600 ml of water are added. The resulting precipitate is sucked off, washed successively with water, little isopropanol and di-isopropyl ether, and dried. The desired product is obtained in a yield of 19.0 g; the substance decomposes above 200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994485
Source datasetuspto-grants-1991_02
ORD IDord-321d38df1c0043a4a5077567961aa3c6
Source noteuspto-grants-1991_02