HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663665Generated: October 30, 2026
Ethyl bromopyruvate → Ethyl 2-(cyanomethyl)-1,3-thiazole-4-carboxylate
https://huagongshe.com/reaction/1663665
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | 2-Cyanoethanethioamide | HCID 1416277 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-(cyanomethyl)-1,3-thiazole-4-carboxylate | HCID 801076 | 26% |
Reaction Steps
To a solution of ethyl 3-bromo-2-oxopropanate (21 g, 110 mmol) in N,N-dimethylformamide (50 mL) was added a solution of 2-cyanoethanethioamide (10 g, 100 mmol) in N,N-dimethylformamide (50 mL) under ice-cooling, and the reaction mixture was stirred at room temperature for 12 hr. The mixture was concentrated under reduced pressure, and the obtained residue was dissolved in ethyl acetate, and washed with 5% aqueous sodium hydrogencarbonate solution and saturated brine. The organic layer was dried over anhydrous sodium sulfate and filtrated. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=20/80→60/40) to give the title compound (5.1 g, 26%) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034812B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-5ad1b55cb1934ca18a27670a5d09af45 |
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| Source note | uspto-grants-2011_10 |
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