Benzophenone → 9-Phenylphenanthrene-1,10-dicarboxylic Anhydride
Reaction equation
[C:1]([O:14]C)(=[O:13])[CH2:2][C:3]1[C:4](=[CH:9][CH:10]=[CH:11][CH:12]=1)[C:5]([O:7]C)=O.[C:16]([C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)(=O)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[C:17]1([C:16]2[C:24]3[C:29]([C:12]4[CH:11]=[CH:10][CH:9]=[C:4]5[C:5](=[O:7])[O:14][C:1](=[O:13])[C:2]=2[C:3]=45)=[CH:28][CH:27]=[CH:26][CH:25]=3)[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1Participants
3
Procedure
As described in example 14, the following compounds were prepared from dimethyl homophthalate and benzophenone:
Sources & evidence
- ORD record
- ord-52fe8c8bf4a647be8f54dacc5bce4879
- Source dataset
- uspto-grants-1995_05
- Patent number
- US05416089
Reaction notes
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