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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630268Generated: November 1, 2026

Aluminium lithium hydride → (4-Ethylthiazol-5-yl)methanol

https://huagongshe.com/reaction/630268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl 4-ethylthiazole-5-carboxylateHCID 53421078—
SolventTetrahydrofuranHCID 8028—
Product(4-Ethylthiazol-5-yl)methanolHCID 5958934771.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. mixture of lithium aluminum hydride (800 mg, 21.0 mmol) in anhydrous THF (30 mL) was slowly added a solution of ethyl 4-ethyl-1,3-thiazole-5-carboxylate (1.91 g, 10.3 mmol) in anhydrous THF (50 mL). The reaction mixture was stirred at 0° C. for 1.5 hours. The reaction was quenched with 5 N NaOH. Water (150 mL) and EtOAc (150 mL) were added. The mixture was stirred for 30 minutes. The solid material was removed by filtration. The organic layer was recovered. The aqueous layer was extracted with EtOAc (1×100 mL). The combined organic extracts were back extracted with brine (2×200 mL), dried over MgSO4, filtered, evaporated, and dried in vacuo, affording (4-ethyl-1,3-thiazol-5-yl)methanol (1.05 g, 71% yield). The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315521B2
Source datasetuspto-grants-2016_04
ORD IDord-c5163d10285f4341876f54d05848ab5f
Source noteuspto-grants-2016_04