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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973866Generated: November 2, 2026

1-(But-3-en-1-yl)-1,4-dihydroanthracene-9,10-dione → 1-Butyl-1,2,3,4-tetrahydroanthracene-9,10-dione

https://huagongshe.com/reaction/1973866

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(But-3-en-1-yl)-1,4-dihydroanthracene-9,10-dioneHCID 21490624—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product1-Butyl-1,2,3,4-tetrahydroanthracene-9,10-dioneHCID 2149062283%

Reaction Steps

A 5.0 g. sample of 1,4-dihydro-1-(3-butenyl)anthraquinone (6a, R = H) was dissolved in 100 ml. of ethyl acetate. The solution was then hydrogenatd using 0.2 g. 10% Pd/C catalyst. After the absorption of three equivalents of hydrogen, the mixture was filtered to remove the catalyst. It was then stirred at room temperature overnight while exposed to air to oxidize the hydroquinone. After removal of the solvent, the residue was recrystallized from methanol to give 4.2 g. product (83% yield). The gas chromatographic retention time, infrared spectrum, and nmr spectrum of this sample were identical with those of an authentic sample.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998937
Source datasetuspto-grants-1976_12
ORD IDord-1a5644cefd8546d790f92726fb870198
Source noteuspto-grants-1976_12