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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877242Generated: November 3, 2026

Thionyl Chloride → HCID 68512244, compound

https://huagongshe.com/reaction/1877242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68513620HCID 68513620—
SolventTolueneHCID 1140—
ProductHCID 68512244HCID 68512244—

Reaction Steps

To a solution of cyclohexyl{2-methyl-5-[4-(trifluoromethyl)phenyl]thiophen-3-yl}methanol (1.20 g) synthesized above in toluene (20 mL) was added thionyl chloride (297 μL), and the mixture was stirred at room temperature for 3 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 (1.27 g, quantitative) as a pale-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-6093d0b7080d488abe7bbaad0e683bd7
Source noteuspto-grants-2012_11