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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099360Generated: October 30, 2026

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

https://huagongshe.com/reaction/1099360

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 3A° 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 numberUS08143424B2
Source datasetuspto-grants-2012_03
ORD IDord-0d836387610f4da99f1bf837610a4755
Source noteuspto-grants-2012_03