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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951536Generated: November 3, 2026

Ethyl Acetate → 1-(4-Ethyl-1,3-thiazol-2-yl)acetone

https://huagongshe.com/reaction/1951536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-Ethyl-2-methylthiazoleHCID 520568—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Ethyl-1,3-thiazol-2-yl)acetoneHCID 59492338—

Reaction Conditions

Temperature-78 °C

Reaction Steps

1.70 g (13.4 mmol) of the compound from example 16A are dissolved in 15 ml of abs. THF and, at −78° C., 5.88 ml (14.7 mmol) of n-butyllithium (2.5 M solution in hexane) are added dropwise. After stirring at −78° C. for 2 hours, 2.00 g (22.7 mmol) of ethyl acetate are added as a solution in 10 ml of abs. THF. The mixture is stirred at −78° C. for 1 h and then warmed to room temperature. It is then hydrolyzed with sodium bicarbonate solution, and the mixture is extracted three times with diethyl ether. The combined organic phases are dried with magnesium sulfate, and the solvent is removed in a rotary evaporator. 1.89 g (84% of theory) of the title compound are obtained. GC-MS (Method 2): Rt=4.20 min; MS (Elpos): m/z=169 [M]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404723B2
Source datasetuspto-grants-2013_03
ORD IDord-143db9d6ee124b54822d8b658be4f104
Source noteuspto-grants-2013_03