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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091407Generated: October 31, 2026

Thionyl Chloride → HCID 66777786, compound

https://huagongshe.com/reaction/2091407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66777714HCID 66777714—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66777786HCID 6677778696%

Reaction Steps

To a solution of [5-(benzyloxy)-3-methyl-1-benzofuran-2-yl](cyclohexyl)methanol (25.17 g) synthesized above in tetrahydrofuran (250 mL) was added thionyl chloride (9.44 mL) at room temperature. The reaction mixture was stirred at room temperature for 1 hr. To the reaction mixture was added aqueous sodium hydrogen carbonate solution cooled to 0° C., and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated to give the title compound (25.39 g, 96%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-008add1b90d3456392ee9f934058c0af
Source noteuspto-grants-2013_05