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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732243Generated: October 29, 2026

Ethanol → 5-Isopropyl-4-(4-Methoxy-Phenyl)-2-Methyl-1,3-Thiazole

https://huagongshe.com/reaction/732243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThioacetamideHCID 2723949—
Reactant2-bromo-1-(4-Methoxy-Phenyl)-3-Methyl-Butan-1-OneHCID 57838362—
SolventEthyl AcetateHCID 8857—
Product5-Isopropyl-4-(4-Methoxy-Phenyl)-2-Methyl-1,3-ThiazoleHCID 5783836351%

Reaction Steps

While 77.0 g of 2-bromo-1-(4-methoxy-phenyl)-3-methyl-butan-1-one (4) prepared in Example 2 were added to 200 ml of ethanol and stirred, 42.7 g of thioacetamide were added. Subsequently, the temperature was gradually increased and stirring under reflux was continued for 22 hr. After the reaction was completed, the resultant reaction mixture was added with 300 ml of ethylacetate, and then washed with a saturated aqueous solution of potassium carbonate. The ethylacetate layer was dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure, thus obtaining 35.8 g (yield: 51.0%) of a title compound as brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585979B2
Source datasetuspto-grants-2009_09
ORD IDord-fbebe0d9b5754199a451b292c063aa26
Source noteuspto-grants-2009_09