Ethyl 3-(4-methoxyphenyl)-2-methylprop-2-enoate → Ethyl 3-(4-methoxyphenyl)-2-methylpropanoate

HRID 1577036Notes

Reaction equation

HRID 1577036 reaction equation
[CH3:1][O:2][C:3]1[CH:16]=[CH:15][C:6]([CH:7]=[C:8]([CH3:14])[C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:5][CH:4]=1.[H][H]>C(O)C.[Pd]>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][CH:8]([CH3:14])[C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:15][CH:16]=1

Participants

5

Reactant 2

HCID 53711494Ethyl 3-(4-methoxyphenyl)-2-methylprop-2-enoateHCID 178418361HCID 178418361, compound

Product 1

HCID 11160380Ethyl 3-(4-methoxyphenyl)-2-methylpropanoate

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

Ethyl p-methoxy-α-methylcinnamate (39.1 g) is dissolved in 186 ml of 2B ethanol. This solution is shaken with 1.5 g of 10% palladium on carbon at an initial pressure of 60 psi until the uptake of hydrogen is 100%. The reaction mixture is removed on an evaporator leaving ethyl β-(p-methoxyphenyl)-α-methylpropionate.

Workup

  1. customThe reaction mixture is removed on an evaporator

Sources & evidence

ORD record
ord-6135eb5c671b4a0fad3c3e36dedc316e
Source dataset
uspto-grants-1976_09
Patent number
US03983253

Reaction notes

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