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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389308Generated: October 30, 2026

Acetylacetone → 3-(7-Methoxy-6-methyl-indan-4-ylmethyl)-pentane-2,4-dione

https://huagongshe.com/reaction/389308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetylacetoneHCID 31261—
Reactant7-Methoxy-6-methyl-indan-4-carbaldehydeHCID 77174827—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventPiperidineHCID 8082—
Product3-(7-Methoxy-6-methyl-indan-4-ylmethyl)-pentane-2,4-dioneHCID 6681299725.2%

Reaction Steps

To the solution of 7-Methoxy-6-methyl-indan-4-carbaldehyde (8.0 gm 0.042 mole) and Acetyl acetone (4.63 gm, 0.046 mole) in Toluene (80 ml), Piperidine (0.5 ml) and Acetic acid (0.5 ml) were added. The reaction mixture was refluxed over 3 A° molecular sieve using dean stark apparatus for 24 hours. Toluene was distilled under vacuum to give a crude product, which was purified by column chromatography using 5% Ethyl acetate in Hexane. The fractions were distilled to give 3.0 gm of condensed product It was dissolved in Methanol (60 ml) and hydrogenation was carried out over 5% w/w Palladium on Barium sulphate (350 mg) at 40-50 psi. using Hydrogen gas at 25-30° C. The reaction mixture was filtered through hyflow bed and distilled under vacuum to give a 2.9 gm of desired compound as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378118B2
Source datasetuspto-grants-2013_02
ORD IDord-3797cb922bcc4c18ab2a8bc6eee3c16b
Source noteuspto-grants-2013_02