Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787713Generated: October 29, 2026

Ethyl isothiocyanate → Cyano-(3-ethyl-4-oxo-thiazolidin-2-yliden)-acetic acid allylester

https://huagongshe.com/reaction/1787713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isothiocyanateHCID 10966—
ReactantSodium hydrideHCID 24758—
ReactantAllyl cyanoacetateHCID 25919—
ReactantBromoacetyl chlorideHCID 89602—
ReactantSodium BicarbonateHCID 516892—
SolventDimethylformamideHCID 6228—
ProductCyano-(3-ethyl-4-oxo-thiazolidin-2-yliden)-acetic acid allylesterHCID 76621903—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 37.6 ml of cyanoacetic acid allyl ester in 60 ml of dimethylformamide is added to a suspension of 12.8 g of sodium hydride (60%) in 200 ml of dimethylformamide at 0° C. It is stirred for 10 more minutes at 0° C., and then a solution of 28.0 ml of ethyl isothiocyanate in 60 ml of dimethylformamide is added. It is then stirred for 2 more hours at 25° C. Then, a solution of 32 ml of bromoacetyl chloride in 60 ml of dimethylformamide is added at 0° C., and it is stirred for 15 more hours at 25° C. Then, the reaction mixture is poured into saturated sodium bicarbonate solution. It is extracted with ethyl acetate, the organic phase is washed with saturated sodium chloride solution, dried on sodium sulfate and concentrated by evaporation in a vacuum. The crude product is purified by column chromatography on silica gel with a mixture that consists of hexane/ethyl acetate. 33.9 g of product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511059B2
Source datasetuspto-grants-2009_03
ORD IDord-51f74bb62445459cbea8a0fe821a842a
Source noteuspto-grants-2009_03