Acetophenone → 2403-28-3
Reaction equation
[C:1]1([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:6]=[CH:5][C:4]([CH:7]=O)=[CH:3][CH:2]=1.[C:15]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)(=[O:17])[CH3:16]>>[C:1]1([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:6]=[CH:5][C:4]([CH:7]=[CH:16][C:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[O:17])=[CH:3][CH:2]=1Participants
3
Procedure
By a procedure similar to that of example 1.59.1, starting from 4-biphenylcarboxaldehyde and acetophenone, 3-(biphenyl-4-yl)-1-phenylprop-2-en-1-one was obtained as yellowish solid.
Sources & evidence
- ORD record
- ord-ef2555d682a9489cb3abb81eac16c314
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912186B2
Reaction notes
Loading…