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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium CyanideHCID 8929—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylateHCID 12603728—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 178418546HCID 178418546—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-cyano-5-phenyl-1,3-thiazole-4-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367696B2
Source datasetuspto-grants-2013_02
ORD IDord-d184072c5da9451f9c16c669c262b828
Source noteuspto-grants-2013_02