HCID 13560734, compound → HCID 21288511, compound

HRID 868432Notes

Reaction equation

HRID 868432 reaction equation
[C:1]([C:8]1[CH:9]=[C:10](/[CH:14]=[CH:15]/[C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:11]=[CH:12][CH:13]=1)(=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].C(C1C=C(/C=C\C2C=CC=CC=2)C=CC=1)(=[O:28])CCCCC>>[C:16]1([CH2:15][CH2:14][CH:10]([CH2:11][CH2:12][CH3:13])[CH2:9][C:8]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)=[O:28])[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1

Participants

3

Reactant 2

HCID 13560734HCID 13560734, compoundHCID 44265511HCID 44265511, compound

Product 1

HCID 21288511HCID 21288511, compound

Procedure

This compound was prepared by the catalytic reduction (H2, 10% Pd-C, ethanol) of either trans-3-hexanoyl stilbene, cis-3-hexanoyl stilbene or, 3-hexanoyl diphenyl acetylene in nearly quantitative yield.

Sources & evidence

ORD record
ord-6dab4d3e41344a4aa63bd2288853cbf2
Source dataset
uspto-grants-1988_10
Patent number
US04778931

Reaction notes

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