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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827885Generated: November 1, 2026

Aluminium lithium hydride → {2-[4-(Trifluoromethyl)phenyl]-1,3-oxazol-4-yl}methanol

https://huagongshe.com/reaction/1827885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 2-(4-(trifluoromethyl)phenyl)oxazole-4-carboxylateHCID 22064320—
SolventTetrahydrofuranHCID 8028—
Product{2-[4-(Trifluoromethyl)phenyl]-1,3-oxazol-4-yl}methanolHCID 22064105—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of methyl 2-[4-(trifluoromethyl)phenyl]-1,3-oxazole-4-carboxylate (1.365 mmol) in tetrahydrofuran (20 ml) was cooled to 0° C., and lithium aluminum hydride in tetrahydrofuran (1.365 mmol) was added dropwise. The reaction mixture was stirred at 0° C. for 30 minutes, slowly quenched with water, followed by addition of ammonium chloride solution. The resulting mixture was filtered through celite, and washed with ethyl acetate. The filtrate was washed with brine, dried over sodium sulfate, and solvent removed under reduced pressure. The residue was purified by chromatography, to yield {2-[4-(trifluoromethyl)phenyl]-1,3-oxazol-4-yl}methan-1-ol, a compound of formula (16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056924B2
Source datasetuspto-grants-2006_06
ORD IDord-504d6449473046a18a20bc4601da4eb5
Source noteuspto-grants-2006_06