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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299702Generated: October 26, 2026

Dimethylformamide → 3-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)phenyl]propanol

https://huagongshe.com/reaction/2299702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(4-Hydroxyphenyl)propanolHCID 82452—
Reactant4-(Chloromethyl)-5-methyl-2-phenyl-1,3-oxazoleHCID 9794289—
SolventWaterHCID 962—
Product3-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)phenyl]propanolHCID 1092535384%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-chloromethyl-5-methyl-2-phenyloxazole (3.41 g), 3-(4-hydroxyphenyl)propanol (2.50 g), potassium carbonate (3.40 g) and N,N-dimethylformamide (25 ml) was stirred for 14 hours at 60° C. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride, dried (MgSO4), and then concentrated. The residue was subjected to column chromatography on silica gel, and 3-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]propanol (4.46 g, yield 84%) was obtained from a fraction eluted with ethyl acetate-hexane (1:1, v/v) as crystals. Recrystallization from ethyl acetate-hexane gave colorless crystals. m.p. 70-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495581B1
Source datasetuspto-grants-2002_12
ORD IDord-0646657eed2d4dc1b0d400b39be85d20
Source noteuspto-grants-2002_12