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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113660Generated: October 27, 2026

Water → 2-butyl-6-methoxy-2-(2-oxopropyl)-3,4-dihydro-1(2H)-naphthalenone

https://huagongshe.com/reaction/2113660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantQuinoneHCID 4650—
ReactantPerchloric AcidHCID 24247—
Reactant2-allyl-2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenoneHCID 58604046—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
Product2-butyl-6-methoxy-2-(2-oxopropyl)-3,4-dihydro-1(2H)-naphthalenoneHCID 58604066—

Reaction Steps

A solution of 2-allyl-2-butyl-6-methoxy-3,4-dihydro-1(2H)-naphthalenone (931 mg, 3.4 mmol) in acetonitrile (10 mL) was treated with benzoquinone (553 mg, 5.12 mmol), palladium(II) acetate (155 mg, 0.69 mmol), water (0.50 mL, 28 mmol), and perchloric acid (70%, ˜0.14 mL, 1.6 mmol). The resulting mixture was stirred overnight at room temperature. The mixture was partitioned between CH2Cl2 (200 mL) and water (100 mL) and the aqueous phase was back-extracted with CH2Cl2 (2×75 mL). The combined organics were washed with brine, dried over MgSO4, filtered, and concentrated under vacuum. The residue (1.17 g) was purified by Biotage™ (Charlottesville, Va.) flash chromatography on a 40S (4×7 cm) silica gel column, eluting with 10:1 to 5:1 hexane-EtOAc. The product-containing fractions were evaporated under vacuum to afford 2-butyl-6-methoxy-2-(2-oxopropyl)-3,4-dihydro-1(2H)-naphthalenone as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432284B2
Source datasetuspto-grants-2008_10
ORD IDord-787cfc2492bd47d0ae9c3bf3d14a5fd4
Source noteuspto-grants-2008_10