Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350000Generated: October 30, 2026

Hydrochloric Acid → 4-(2-Phenyl-4-oxazolylmethoxy)benzylalcohol

https://huagongshe.com/reaction/350000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(2-Phenyl-4-oxazolylmethoxy)benzaldehydeHCID 10826513—
SolventWaterHCID 962—
Product4-(2-Phenyl-4-oxazolylmethoxy)benzylalcoholHCID 2302488891%

Reaction Steps

Sodium borohydride (0.36 g) was added to a mixture of 4-(2-phenyl-4-oxazolylmethoxy)benzaldehyde (2.65 g) and methanol (50 ml) under ice-cooling, which was stirred at room temperature for 1 hour. Dilute hydrochloric acid and water were added to the reaction mixture, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4) and concentrated to obtain 4-(2-phenyl-4-oxazolylmethoxy)benzyl alcohol (2.43 g, yield 91%) as colorless crystals. This was recrystallized from ethyl acetate-hexane. Melting point: 141–142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-93ce78c37ffa4b52a7cc5359d8df1b12
Source noteuspto-grants-2007_02