Benzyl Bromide → 1-(4-Bromophenyl)-2-phenylethanone
Reaction equation
[CH2:1](Br)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Br:9][C:10]1[CH:18]=[CH:17][C:13]([C:14](Cl)=[O:15])=[CH:12][C:11]=1C.BrC1C=CC(C(Cl)=O)=CC=1>>[Br:9][C:10]1[CH:11]=[CH:12][C:13]([C:14](=[O:15])[CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:17][CH:18]=1Participants
4
Procedure
The title compound was prepared according to the procedure of step 1 in the Example 169 using benzyl bromide and 4-bromo-3-methylbenzoyl chloride, instead of 4-bromobenzoyl chloride.
Sources & evidence
- ORD record
- ord-739e177a0a9a4fdebc256e642dff9bd8
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06608095B2
Reaction notes
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