Acetophenone → HCID 238617, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[Cl:10])[CH:5]=O.[C:11]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)(=[O:13])[CH3:12]>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:5]=[CH:12][C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[O:13])[CH:7]=[CH:8][C:9]=1[Cl:10]Participants
3
Procedure
By a procedure similar to that of example 1.59.1, starting from 3,4-dichlorobenzaldehyde and acetophenone, 3-(3,4-dichlorophenyl)-1-phenylprop-2-en-1-one was obtained as yellowish solid.
Sources & evidence
- ORD record
- ord-4c7982fee3b44fa3aba3a21a335979ac
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912186B2
Reaction notes
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