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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893217Generated: November 1, 2026

Hydrochloric Acid → 4-(Benzo[D][1,3]dioxol-5-YL)cyclohex-3-enone

https://huagongshe.com/reaction/1893217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Benzo[1,3]dioxol-5-yl-4-hydroxycyclohexanoneHCID 15199689—
SolventTetrahydrofuranHCID 8028—
Product4-(Benzo[D][1,3]dioxol-5-YL)cyclohex-3-enoneHCID 59541914—

Reaction Steps

A solution of 4-benzo[1,3]dioxol-5-yl-4-hydroxy-cyclohexanone (as prepared in the previous step, 3.5 g, 15 mmol) in THF (10 mL) was treated with 6N HCl (5 mL) overnight under argon at room temperature. The resulting solution was quenched with sufficient 1N NaOH to neutralize the reaction. The solvent was removed and the residue was partitioned between DCM and water. The organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated to give a yellow oil, which was then purified by silica gel column on a CombiFlash® system using hexanes and ethyl acetate (from 10% ethyl acetate to 100% ethyl acetate) to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513229B2
Source datasetuspto-grants-2013_08
ORD IDord-f3f6f92178074950b773e80510465149
Source noteuspto-grants-2013_08