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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794329Generated: November 4, 2026

Thionyl Chloride → HCID 22221286, compound

https://huagongshe.com/reaction/1794329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 22221119HCID 22221119—
SolventTolueneHCID 1140—
ProductHCID 22221286HCID 2222128681%

Reaction Steps

To a solution of 5-(2,4-difluorophenyl)-4-isoxazolylmethanol (2.50 g) in toluene (50 ml) was added dropwise thionyl chloride (2.11 g) at 0° C., and the mixture was stirred at room temperature for 1 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-(2,4-difluorophenyl)isoxazole (2.20 g, yield 81%) was obtained as an oil from a fraction eluted with ethyl acetate-hexane (1:5, volume ratio). NMR (CDCl3) δ: 4.53 (2H, s), 6.95–7.15 (2H, m), 7.6–7.75 (1H, m), 8.43 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022725B2
Source datasetuspto-grants-2006_04
ORD IDord-aa275bb5fd40409caa6cdb316732db7b
Source noteuspto-grants-2006_04