HCID 15173989, compound → 1-Ethyl-2-(2-methylpropyl)benzene
Reaction equation
[CH2:1]([C:5]1[CH:12]=[CH:11][CH:10]=[CH:9][C:6]=1[CH:7]=[CH2:8])[CH:2]([CH3:4])[CH3:3]>[Pd]>[CH2:1]([C:5]1[CH:12]=[CH:11][CH:10]=[CH:9][C:6]=1[CH2:7][CH3:8])[CH:2]([CH3:4])[CH3:3]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
In a 1-liter autoclave equipped with a stirrer were placed 35.8 g of a 10% palladium black catalyst and all of the above-mentioned crude o-isobutylstyrene, and hydrogenation was carried out at a reaction temperature of 50° C. under a hydrogen pressure of 20 kg/cm2. After hydrogen had not been absorbed any more, the used catalyst was removed from the reaction mixture by filtration, followed by distillation, thereby obtaining 642 g of o-isobutylethylbenzene having 99.8% purity.
Workup
- customIn a 1-liter autoclave equipped with a stirrer
- customwas carried out at a reaction temperature of 50° C. under a hydrogen
- customAfter hydrogen had not been absorbed any more, the used catalyst
- customwas removed from the reaction mixture by filtration
- distillationfollowed by distillation
Sources & evidence
- ORD record
- ord-de07d6b175934bb399e6c849b06294c1
- Source dataset
- uspto-grants-1992_03
- Patent number
- US05097061
Reaction notes
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