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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090976Generated: October 31, 2026

Thionyl Chloride → HCID 63433147, compound

https://huagongshe.com/reaction/2090976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 61088367HCID 61088367—
SolventTolueneHCID 1140—
ProductHCID 63433147HCID 6343314797%

Reaction Steps

To a solution of 1-benzothiophen-3-yl(cyclohexyl)methanol (2.32 g) synthesized above in toluene (25 mL) was added dropwise thionyl chloride (824 μL), and the mixture was stirred at room temperature for 4 hr. The reaction mixture was poured into ice-cooled saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give the title object compound (2.42 g, 97%) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-e4e6a3b29b8a437bb83dccbd08cf9259
Source noteuspto-grants-2013_05