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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794338Generated: November 2, 2026

Thionyl Chloride → HCID 22221447, compound

https://huagongshe.com/reaction/1794338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 22221006HCID 22221006—
SolventTolueneHCID 1140—
ProductHCID 22221447HCID 2222144753%

Reaction Steps

To a solution of 5-(2,5-dichlorophenyl)-4-isoxazolylmethanol (3.80 g) in toluene (60 ml) was added dropwise thionyl chloride (2.78 g) at 0° C. and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated, saturated aqueous sodium hydrogencarbonate was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and 4-chloromethyl-5-(2,5-dichlorophenyl)isoxazole (2.15 g, yield 53%) was obtained as an oil from a fraction eluted with ethyl acetate-hexane (1:9, volume ratio). NMR (CDCl3) δ: 4.45 (2H, s), 7.4–7.55 (3H, m), 8.48 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022725B2
Source datasetuspto-grants-2006_04
ORD IDord-46fde503cdc446d9aa62df1daf6854d7
Source noteuspto-grants-2006_04