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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635595Generated: October 30, 2026

Hydrochloric Acid → 3,4-dihydro-4,4-dimethyl-7-acetyl-1(2H)-naphthalenone

https://huagongshe.com/reaction/635595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactant7-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-oneHCID 10753357—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
Product3,4-dihydro-4,4-dimethyl-7-acetyl-1(2H)-naphthalenoneHCID 22323726—

Reaction Steps

A solution of 4,4-dimethyl-7-bromo-3,4-dihydronaphthalen-1(2H)one (Compound G) (1.78 g, 7 mmol), 1-ethoxyyinyltributyltin (EVTB) (3.3 g, 9.12 mmol), bis(triphenylphosphine)palladium(II)chloride (260 mg, 0.23 nmol) in THF (25 mL) was refluxed for 24 h under argon atmosphere. To the reaction, additional EVTB (1.5 g, 4.1 mmol) and bis(triphenylphosphine)palladium(II)chloride (200 mg, 0.2 mmol) were added and the mixture was and refluxed for an additional 24 h. The reaction mixture was cooled to room temeperature and 10% hydrochloric acid (10 ml) was added. After 10 min, the mixture was extracted with ether (3×50 mL), the combined organic layer was washed with water (10 mL), 10% sodiumbicarbonate (10 mL), brine (10 mL), dried with magnesium sulfate. Solvent was removed under reduced pressure, and after purification by flash chromatography the title compound was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06187933B1
Source datasetuspto-grants-2001_02
ORD IDord-d57dd7ff662f4da09a13f4c17909bd7b
Source noteuspto-grants-2001_02