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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794321Generated: October 30, 2026

Thionyl Chloride → HCID 22221311, compound

https://huagongshe.com/reaction/1794321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 22221040HCID 22221040—
ProductHCID 22221311HCID 2222131192%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 3-(4-phenylphenyl)-4-isoxazolylmethanol (4.16 g) and thionyl chloride (10.0 ml) was stirred at 0° C. for 30 min. The reaction mixture was concentrated, and saturated aqueous sodium hydrogencarbonate was added to the residue. The mixture was extracted with ethyl acetate and the ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained colorless crystals were filtrated to give 4-chloromethyl-3-(4-phenylphenyl)isoxazole (3.84 g, yield 92%). The crystals were recrystallized from ethyl acetate-hexane. melting point: 102–103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022725B2
Source datasetuspto-grants-2006_04
ORD IDord-ac7d6558fd584483b738b97314bc88a3
Source noteuspto-grants-2006_04