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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877217Generated: November 1, 2026

Thionyl Chloride → HCID 63432053, compound

https://huagongshe.com/reaction/1877217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 61088924HCID 61088924—
SolventTolueneHCID 1140—
ProductHCID 63432053HCID 6343205394%

Reaction Steps

To a solution of cyclohexyl(2,5-dimethylthiophen-3-yl)methanol (643 mg) synthesized above in toluene (10 mL) was added thionyl chloride (314 μL), and the mixture was stirred at room temperature for 6 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 compound (653 mg, 94%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-31dcc03a9fc5421aad75ad45431b2f0a
Source noteuspto-grants-2012_11