HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383931Generated: October 26, 2026
Sulfuric Acid → Ethyl 2-cyano-5-phenyl-1,3-thiazole-4-carboxylate
https://huagongshe.com/reaction/383931
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylate | HCID 12603728 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-cyano-5-phenyl-1,3-thiazole-4-carboxylate | HCID 59291286 | — |
Reaction Steps
To a mixed solution of ethyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylate, acetic acid, and sulfuric acid was slowly added an aqueous NaNO2 solution (5 mL) at 0° C., followed by stirring at the same temperature for 1 hour. This solution was added to an aqueous solution (40 mL) containing CuCN, NaCN, and NaHCO3 (30 g) over 30 minutes, followed by stirring at the same temperature for 1 hour. EtOAc was added thereto, and the insolubles were filtered through Celite. The filtrate was extracted with EtOAc, the organic layer was dried, and the solvent was removed by evaporation under reduced pressure. The residue was purified by silica gel column chromatography (hexane:EtOAc=from 5:1 to 3:1 to 2:1) to obtain ethyl 2-cyano-5-phenyl-1,3-thiazole-4-carboxylate as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367696B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-d184072c5da9451f9c16c669c262b828 |
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| Source note | uspto-grants-2013_02 |
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