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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77644Generated: October 26, 2026

4-Methyl-1,7-diphenyl-1,6-heptadiene-3,5-dione → 4-Methyl-1,7-diphenylheptane-3,5-dione

https://huagongshe.com/reaction/77644

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-1,7-diphenyl-1,6-heptadiene-3,5-dioneHCID 69501726—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-Methyl-1,7-diphenylheptane-3,5-dioneHCID 6950177273%

Reaction Steps

4-Methyl-1,7-diphenyl-1,6-hetpadiene-3,5-dione (6b, 0.96 g, 3.3 mmol) and palladium on activated carbon (0.25 g, 10%) were combined in ethyl acetate (50 ml). The mixture was placed under a hydrogen atmosphere (60 psi) on a Parr apparatus for 2 hr at room temperature. The resulting mixture was filtered through celite and the filtrate was washed with saturated sodium chloride, dried over magnesium sulfate, filtered and evaporated to afford an oil. The crude oil was twice chromatographed on silica gel with ethyl acetate/hexane to give an oil. The oil was distilled bulb to bulb to give 0.71 g (73%) of a clear oil; 1H NMR: δ enol form: 1.66 (s, 3H), 2.73 (m, 8H), 7.17 (m, 10H); keto form: 1.20 (d, 3H, J=7.2 Hz), 2.73 (m, 8H), 3.55 (q, 1H, J=7.0 Hz), 7.17 (m, 10H); 13C NMR: δ 12.3, 29.3, 31.0, 37.6, 42.8, 60.9, 104.2, 125.9, 128.1, 128.2, 140.4, 140.8, 174.6, 191.5, 205.6; Exact mass calcd for C20H22O2: 294.1620, observed (M+H) 295.1693.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841326B2
Source datasetuspto-grants-2014_09
ORD IDord-5ba5e6758e0847e2b39eb70ee3868ed4
Source noteuspto-grants-2014_09