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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254171Generated: October 31, 2026

Acetic Acid → Ethyl 3-(4-methyl-1,3-thiazol-2-yl)-3-oxopropanoate

https://huagongshe.com/reaction/254171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiethyl CarbonateHCID 7766—
ReactantSodium hydrideHCID 24758—
Reactant2-Acetyl-4-methylthiazoleHCID 5324797—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solvent2-MethylpentaneHCID 7892—
ProductEthyl 3-(4-methyl-1,3-thiazol-2-yl)-3-oxopropanoateHCID 6684687974%

Reaction Conditions

Temperature80 °C

Reaction Steps

NaH (60% in oil, 1.34 g, 33.5 mmol) was washed with isohexane (2×14 mL), suspended in toluene (25 mL), treated with diethyl carbonate (4.7 mL, 4.6 g, 38.8 mmol), heated to 80° C., treated dropwise over 20 min with a solution of 2-acetyl-4-methylthiazole (2.72 g, 19.2 mmol) in toluene (5 mL) and stirred at 80° C. for 2 h. The mixture was cooled to 0° C., treated dropwise with HOAc (4.65 mL, 4.9 g, 81 mmol) followed by ice (25 g) and water (50 mL) and stirred for 30 min. The aqueous phase was extracted with toluene (50 mL), the combined organic phase was washed with water (50 mL), dried (MgSO4) and concentrated in vacuo to give the crude product (3 g, 74%) as a dark red oil, used in the next step without further purification; NMR δH (400 MHz, CDCl3) 1.26 (3H, t, J 7.2 Hz), 2.92 (3H, s), 4.14 (2H, s), 4.18-4.25 (2H, m) and 7.31 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875600B2
Source datasetuspto-grants-2011_01
ORD IDord-f39492cb4dc843edad1063bf49cffa23
Source noteuspto-grants-2011_01