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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381273Generated: October 25, 2026

Ethyl 2-((dimethylamino)methyl)thiazole-4-carboxylate → (2-((Dimethylamino)methyl)thiazol-4-yl)methanol

https://huagongshe.com/reaction/381273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-((dimethylamino)methyl)thiazole-4-carboxylateHCID 2039211—
ReactantAluminium lithium hydrideHCID 21226445—
Product(2-((Dimethylamino)methyl)thiazol-4-yl)methanolHCID 183802062%

Reaction Conditions

Temperature7.5 °C

Reaction Steps

To a mixture of lithium aluminum hydride (4.5 g, 119 mmol) in ice cold tetrahydrofuran (100 mL) was added ethyl2-dimethylaminomethylthiazole-4-carboxylate (8.5 g, 39.7 mmol in 40 mL of tetrahydrofuran) dropwise over 40 min maintaining an internal temperature of 5-10° C. The mixture was stirred at this temperature range for 90 min. The reaction was carefully quenched with saturated aqueous ammonium chloride (30 mL). The resulting gray slurry was stirred 15 min and filtered through celite. The pad was well washed with ethyl acetate. The filtrate was washed with brine and dried over sodium sulfate. Concentration of this organic solution gave 4.2 g (62%) of 2-dimethylaminomethyl-4-hydroxymethylthiazole as an amber oil which had NMR δ 7.12 (s, 1 H), 4.71 (s, 2 H), 3.73 (s, 2 H), 2.50 (br s, 1 H), 2.32 (s, 6 H). The material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306864B1
Source datasetuspto-grants-2001_10
ORD IDord-7dc3932d869e4baf9c763bdea79f81d1
Source noteuspto-grants-2001_10