3-Methyl-2-butanone → 1-(4-Benzyloxyphenyl)-4-methyl-pent-1-en-3-one
Reaction equation
[CH3:1][CH:2]([CH3:6])[C:3](=[O:5])[CH3:4].[CH2:7]([O:14][C:15]1[CH:22]=[CH:21][C:18]([CH:19]=O)=[CH:17][CH:16]=1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[OH-].[Ba+2].[OH-]>CCO>[CH2:7]([O:14][C:15]1[CH:16]=[CH:17][C:18]([CH:19]=[CH:4][C:3](=[O:5])[CH:2]([CH3:6])[CH3:1])=[CH:21][CH:22]=1)[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared as described in the General Method 2 using 81.1 g (942 mmol) of 3-methyl-butan-2-one, 100 g (474 mmol) of 4-benzyloxy benzaldehyde, 10 g of anhydrous barium hydroxide and 500 mL of EtOH.
Sources & evidence
- ORD record
- ord-5e5820244c6543a186f4751729a479ae
- Source dataset
- uspto-grants-1998_11
- Patent number
- US05834506
Reaction notes
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