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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl isothiocyanate | HCID 10966 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Allyl cyanoacetate | HCID 25919 | — |
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Cyano-(3-ethyl-4-oxo-thiazolidin-2-yliden)-acetic acid allylester | HCID 76621903 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511059B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-51f74bb62445459cbea8a0fe821a842a |
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| Source note | uspto-grants-2009_03 |
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