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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860586Generated: October 30, 2026

Diethyl Ether → 1-[4-Ethyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-yl]-ethanol

https://huagongshe.com/reaction/860586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant4-Ethyl-2-(4-trifluoromethyl-phenyl)-oxazole-5-carbaldehydeHCID 58765704—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1-[4-Ethyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-yl]-ethanolHCID 58765801—

Reaction Steps

To a solution of 4-ethyl-2-(4-trifluoromethyl-phenyl)-oxazole-5-carbaldehyde (0.793 g, 2.95 mmole) in THF (30 mL) at 0° C., is added a solution of methyl magnesium bromide in diethyl ether (3.0M, 2.0 mL, 0.60 mmole) dropwise. The reaction is stirred for 5 minutes and then warmed up to room temperature for 30 minutes. The reaction is quenched with NH4Cl(aq) (10 mL), partitioned between ethyl acetate (50 mL) and water (50 mL). Extracted the aqueous layer with ethyl acetate (2×50 mL). The combined organic is washed with brine (3×100 mL), dried over Na2SO4, filtered and concentrated to provide the titled compound as a white solid. The crude product is used for the next step without further purification. Mass [EI+] 286 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153878B2
Source datasetuspto-grants-2006_12
ORD IDord-ddcb37fafce74f7d866b5505955fb75c
Source noteuspto-grants-2006_12