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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257476Generated: October 30, 2026

Thionyl Chloride → HCID 19783302, compound

https://huagongshe.com/reaction/257476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 19783305HCID 19783305—
ProductHCID 19783302HCID 1978330236.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

To the said solid, that is, 1.59 g (6.49 mmol) of 1-(2-fluorophenyl)-3-(4-pyridyl)-2-butanol, 2.5 ml of thionyl chloride was added and stirred for one hour at 40° C. After distilling away excessive thionyl chloride under reduced pressure, water was added and the residue was alkalized with sodium carbonate and was extracted with ethyl acetate. After drying over anhydrous sodium sulfate, ethyl acetate was distilled away under reduced pressure to obtain a brown oily substance. The resulting oily substance was purified by silica gel column chromatography to obtain 0.54 g of the desired compound (yield: 31.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262420
Source datasetuspto-grants-1993_11
ORD IDord-1d5fe70ccd91474db0ddf7bfd8c7a36f
Source noteuspto-grants-1993_11