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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058353Generated: October 26, 2026

Ethyl Acetate → (Dimethyl-1,3-thiazol-5-yl)methanol

https://huagongshe.com/reaction/1058353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantEthyl 2,4-dimethylthiazole-5-carboxylateHCID 603810—
ReactantPotassium sodium tartarateHCID 9855836—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product(Dimethyl-1,3-thiazol-5-yl)methanolHCID 277625091%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of lithium aluminum hydride (563 mg, 14.8 mmol) in diethyl ether (25 mL) at 0° C. was added ethyl-2,4-dimethylthiazole-5-carboxylate (2.5 g, 13.5 mmol) in three portions. The reaction mixture was allowed to stir at 0° C. for 10 min, then at room temperature for 24 h. Ethyl acetate (65 mL) was added very slowly dropwise at 0° C. The reaction mixture was then added slowly to an aqueous solution of potassium sodium tartrate (30% w/v; 20 mL) and stirred for 2 h. The layers were separated and the aqueous layer was re-extracted with ethyl acetate (1×30 mL). The combined organic layers were dried (MgSO4), filtered, evaporated under reduced pressure. The resulting colorless solid was dried under high vacuum to give 2,4-dimethylthiazole-5-methanol (1.7 g, 91% yield). This material was used in a subsequent step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515124B2
Source datasetuspto-grants-2003_02
ORD IDord-d85fac8774ac422582c6725eb42a1bd3
Source noteuspto-grants-2003_02