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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091122Generated: October 30, 2026

Thionyl Chloride → HCID 66778915, compound

https://huagongshe.com/reaction/2091122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66778911HCID 66778911—
SolventTolueneHCID 1140—
ProductHCID 66778915HCID 66778915—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution (10 mL) of (5-chloro-3-methyl-1-benzofuran-2-yl)(cyclohexyl)methanol (518 mg) synthesized above in toluene was added thionyl chloride (163 μL), and the mixture was stirred at 100° C. 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 object compound (553 mg, quantitative) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-847bb386c41d4ecd850e2517b345a019
Source noteuspto-grants-2013_05