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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178213Generated: November 3, 2026

Ethyl Acetate → 2-Acetyl-4,5-dimethylthiazole

https://huagongshe.com/reaction/1178213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4,5-DimethylthiazoleHCID 62510—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product2-Acetyl-4,5-dimethylthiazoleHCID 275627266%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of 4,5-dimethylthiazole (2.0 g, 17.67 mmol, 1 eq.) in dry diethyl ether (20 mL) was added slowly dropwise, over approximately 30 minutes, to a solution of butyllithium (7.8 mL, 19.44 mmol, 2.5M, 1.1 eq.) in dry diethyl ether (20 mL) at −70° C. The resultant solution was stirred at −70° C. for 30 minutes, −30° C. for 20 minutes and then re-cooled to −70° C. Dry ethyl acetate (3.11 g, 3.5 mL, 35.34 mmol, 2 eq.) was added in one portion to the deep red solution and the cooling bath was removed. After 50 minutes stirring at room temperature the reaction mixture was poured into saturated NaHSO4 and extracted with ethyl acetate (3×50 mL). The combined organic extracts were washed with saturated Na2CO3 (1×50 mL), brine (1×50 mL), dried over solid Na2SO4 and filtered. The filtrate was concentrated under reduced pressure and the resultant greenish, mobile oil was purified by column chromatography (15% ethyl acetate in hexanes) on silica gel giving a yellow oil (1.81 g, 66% yield): 1H (400 Mhz, CDCl3) δ 2.4(3H, s), 2.5(3H, s), 2.7(3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276502B2
Source datasetuspto-grants-2007_10
ORD IDord-ba49d759284942aaa41b66912a83b7d0
Source noteuspto-grants-2007_10