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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070081Generated: November 2, 2026

Thionyl Chloride → 4-(2-Chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole

https://huagongshe.com/reaction/1070081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 10957398HCID 10957398—
SolventTolueneHCID 1140—
Product4-(2-Chloromethylphenoxymethyl)-5-methyl-2-phenyloxazoleHCID 11099036—

Reaction Steps

Thionyl chloride (1.69 g) was added dropwise to a stirred suspension of 2-(5-methyl-2-phenyl4-oxazolylmethoxy)benzyl alcohol (4.00 g) in toluene (60 ml) at 0° C. After stirring at room temperature for 2 hours, the reaction mixture was concentrated. The residual crystals were dissolved in ethyl acetate and washed with aqueous sodium bicarbonate and water. The ethyl acetate layer was separated, dried (MgSO4), and concentrated to give 4-(2-chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole as crystals. Recrystallization from ethyl acetate-hexane gave colorless needles (3.50 g, yield 82%). m.p. 103-104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251926B1
Source datasetuspto-grants-2001_06
ORD IDord-9d57748de5244c76a535a9a1be5cb7bc
Source noteuspto-grants-2001_06