Benzaldehyde → HCID 2794969, compound
Reaction equation
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:9]([C:12]1[CH:25]=[CH:24][C:23]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[CH:16]=[CH:15][C:14]=2[CH:13]=1)(=[O:11])[CH3:10]>>[CH:13]1[C:14]2[CH:15]=[CH:16][C:17]3[C:22](=[CH:21][CH:20]=[CH:19][CH:18]=3)[C:23]=2[CH:24]=[CH:25][C:12]=1[C:9](=[O:11])[CH:10]=[CH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
By a procedure similar to that of example 1.59.1, starting from benzaldehyde and commercial 2-acetylphenanthrene, 1-(2-phenanthrenyl)-3-phenylprop-2-en-1-one was obtained as yellowish solid.
Sources & evidence
- ORD record
- ord-40aaa8db324f409b88599499135cd2c5
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912186B2
Reaction notes
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