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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221520Generated: October 26, 2026

Ethanol → (4-{[2-(2-Furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-(methoxymethoxy)phenyl)methanol

https://huagongshe.com/reaction/2221520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant4-{[2-(2-Furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-(methoxymethoxy)benzaldehydeHCID 23076616—
SolventTetrahydrofuranHCID 8028—
Product(4-{[2-(2-Furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-(methoxymethoxy)phenyl)methanolHCID 6921520991%

Reaction Steps

To a solution of 4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-(methoxymethoxy)benzaldehyde (15.50 g) in tetrahydrofuran (100 mL)-ethanol (50 mL) was gradually added sodium borohydride (1.71 g) at 0° C. After stirring at room temperature for 2 hrs, water was added to the reaction mixture, 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 (4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-(methoxymethoxy)phenyl)methanol as colorless crystals (14.11 g, yield 91%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 92-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-cdaaf4d5ec7844848119589932aa5f07
Source noteuspto-grants-2008_05