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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877204Generated: November 2, 2026

Thionyl Chloride → HCID 68514363, compound

https://huagongshe.com/reaction/1877204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68511594HCID 68511594—
SolventTolueneHCID 1140—
ProductHCID 68514363HCID 6851436392%

Reaction Steps

To a solution of 4-{4-[cyclohexyl(hydroxy)methyl]-5-ethylthiophen-2-yl}tetrahydro-2H-thiopyran-4-ol (532 mg) synthesized in Example 85 (3) in toluene (10 mL) was added thionyl chloride (137 μL), and the mixture was stirred at room temperature for 1 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 (491 mg, 92%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-9c1f1b6639c44b2d81828ec32c224ce2
Source noteuspto-grants-2012_11