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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072388Generated: November 2, 2026

Aluminium lithium hydride → (2-Ethyl-1,3-thiazol-5-yl)methanol

https://huagongshe.com/reaction/2072388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 21408257HCID 21408257—
SolventTetrahydrofuranHCID 8028—
Product(2-Ethyl-1,3-thiazol-5-yl)methanolHCID 2140825894.2%

Reaction Steps

2.4 g of mixed lithium aluminum hydride was added under nitrogen to a solution of 11.3 g of methyl 2-ethyl-thiazole-5-carboxylate in 100 ml of anhydrous tetrahydrofuran at 20 to 25° C and the mixture was refluxed for 1 1/2 hours. After cooling the mixture, excess lithium aluminum hydride was destroyed by the addition of ethyl acetate. The mixture was added to water and was vacuum filtered. The recovered precipitate was empasted with ethyl acetate and then with a methanol-methylene chlorine mixture. The filtrate was washed with water, dried and evaporated to dryness to obtan 9.5 g of an oil which was rectified under reduced pressure to obtain 8.9 g of 2-ethyl-thiazole-5-methanol with a boiling point of 78° C at 0.1 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04051249
Source datasetuspto-grants-1977_09
ORD IDord-49c31ad84948443cb38705d0e2a7dc76
Source noteuspto-grants-1977_09