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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294169Generated: October 26, 2026

Ethanol → [2-[3-Methoxy-4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]-3-pyridyl]methanol

https://huagongshe.com/reaction/1294169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant2-[3-Methoxy-4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]nicotinaldehydeHCID 86591563—
SolventWaterHCID 962—
Product[2-[3-Methoxy-4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]-3-pyridyl]methanolHCID 6888397299%

Reaction Steps

To a mixture of 2-[3-methoxy-4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]nicotinaldehyde (620 mg), tetrahydrofuran (10 ml) and ethanol (10 mL) was added sodium borohydride (54 mg) at 0° C., and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added water and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated to give crystals (615 mg, 99%) of [2-[3-methoxy-4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]-3-pyridyl]methanol. The crystals were recrystallized from ethyl acetate-hexane. melting point: 143-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238716B2
Source datasetuspto-grants-2007_07
ORD IDord-91538a24d1a64eba8874a8125d329815
Source noteuspto-grants-2007_07