Benzyl Bromide → Benzyl 7-oxooctanoate
Reaction equation
[O:1]=[C:2]([CH3:11])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]([OH:10])=[O:9].[CH2:12](Br)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[O:1]=[C:2]([CH3:11])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]([O:10][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:9]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Benzyl 7-oxooctanoate was prepared by benzylation of 7-oxooctanoic acid with benzyl bromide and potassium carbonate in dimethyl formamide.
Sources & evidence
- ORD record
- ord-c4bb80abbe704cb6b9de76dd9722654e
- Source dataset
- uspto-grants-1993_09
- Patent number
- US05248810
Reaction notes
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