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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299732Generated: October 30, 2026

Toluene → 4-(3-Chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole

https://huagongshe.com/reaction/2299732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantThionyl ChlorideHCID 24386—
Reactant{3-[(5-Methyl-2-Phenyl-1,3-Oxazol-4-Yl)methoxy]phenyl}methanolHCID 11140977—
SolventWaterHCID 962—
Product4-(3-Chloromethylphenoxymethyl)-5-methyl-2-phenyloxazoleHCID 1088155184%

Reaction Steps

Thionyl chloride (4.45 ml) was added dropwise to a mixture of 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzylalcohol (15.0 g) and toluene (200 ml) at 0° C. After stirring at room temperature for 1 hour, water was added to the reaction mixture and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The remaining crystals were recrystallized from ethyl acetate-hexane to obtain 4-(3-chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole (13.4 g, yield 84%) as pale-yellow crystals. m.p. 79-80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495581B1
Source datasetuspto-grants-2002_12
ORD IDord-72b8ec38bd844163ba48e4712a183583
Source noteuspto-grants-2002_12