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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244624Generated: October 31, 2026

Thioacetamide → Ethyl 2-methyl-5-(1-methylethyl)-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/244624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioacetamideHCID 2723949—
ReactantEthyl 3-bromo-4-methyl-2-oxopentanoateHCID 58356425—
SolventEthanolHCID 702—
ProductEthyl 2-methyl-5-(1-methylethyl)-1,3-thiazole-4-carboxylateHCID 5835635162.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of thioacetamide (158 mg) in ethanol (20 ml) was added ethyl 3-bromo-4-methyl-2-oxopentanoate (500 mg) in ethanol (0.5 ml). Molecular sieves (100 mg) were added and the mixture was heated at 80° C. for 18 h. The mixture was filtered, washing with ethanol (5 ml) and the solvent removed in vacuo. The residue triturated with DCM and the solid removed by filtration. The filtrate was concentrated to ˜5 ml and purified by column chromatography on silica gel (10 g silica), eluting with a gradient of 0-100% ethyl acetate in cyclohexane to give the title compound as a yellow oil (280 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658635B2
Source datasetuspto-grants-2014_02
ORD IDord-6e39d18be1de4aca94da424273dadef3
Source noteuspto-grants-2014_02