3-(4-Bromophenyl)-1-phenylpropan-1-one → HCID 44220691, compound
Reaction equation
BrC1C=CC(CCC(C2C=CC=CC=2)=O)=CC=1.[Br:18][C:19]1[CH:24]=[CH:23][C:22]([CH2:25][CH2:26]/[C:27](/[C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)=[CH:28]/[C:29]([O:31][CH2:32][CH3:33])=[O:30])=[CH:21][CH:20]=1>>[Br:18][C:19]1[CH:20]=[CH:21][C:22]([CH2:25][CH2:26]/[C:27](/[C:34]2[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=2)=[CH:28]\[C:29]([O:31][CH2:32][CH3:33])=[O:30])=[CH:23][CH:24]=1Participants
3
Procedure
By a procedure similar to that of example 1.85.3, starting from 3-(4-bromophenyl)-1-phenylpropan-1-one, (Z)-ethyl 5-(4-bromophenyl)-3-phenylpent-2-enoate and (E)-ethyl 5-(4-bromophenyl)-3-phenylpent-2-enoate were obtained as colourless oils.
Sources & evidence
- ORD record
- ord-2dd913cad43941ddacb38b226b0d4de1
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912186B2
Reaction notes
Loading…