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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644005Generated: October 26, 2026

Methyl 4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]benzoate → 4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyl alcohol

https://huagongshe.com/reaction/644005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]benzoateHCID 11461459—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyl alcoholHCID 11022807—

Reaction Conditions

Temperature0 °C

Reaction Steps

Lithium aluminum hydride (15.5 mL of a 1.0 M solution in THF) is added slowly to a cooled (ice-water bath) solution of the title B compound, 4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-benzoic acid methyl ester (2.0 g, 6.18 mmol) in THF (30 mL). The mixture is stirred at 0° C. for 3 h, then quenched with saturated sodium bicarbonate, and extracted with EtOAc. The organic solution is washed with brine, dried over magnesium sulfate, and concentrated under vacuum to give the crude product. The product is purified by silica gel chromatography using 30% EtOAc in hexane as the eluent to give [4-(5-methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl]-methanol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700637B2
Source datasetuspto-grants-2010_04
ORD IDord-b3bd0b1ad8524663a3d75ea4da848814
Source noteuspto-grants-2010_04