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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091172Generated: November 2, 2026

Thionyl Chloride → HCID 66777958, compound

https://huagongshe.com/reaction/2091172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66777987HCID 66777987—
SolventTolueneHCID 1140—
ProductHCID 66777958HCID 6677795890%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution (20 mL) of (3-bromo-5-methoxy-1-benzofuran-2-yl)(cyclohexyl)methanol (1.82 g) synthesized above in toluene was added thionyl chloride (469 μL) and the mixture was stirred at 100° C. for 1.5 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 (1.73 g, 90%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-e2118fc61d7d4c5eb368bddc8845866c
Source noteuspto-grants-2013_05