Phthalimide → HCID 21555843, compound
Reaction equation
[F:1][C:2]([F:25])([F:24])[C:3]1[CH:4]=[CH:5][C:6]([N:17]2[CH:21]=[CH:20][N:19]=[C:18]2[CH2:22]O)=[C:7]([CH:16]=1)[C:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:9].[C:26]1(=[O:36])[NH:30][C:29](=[O:31])[C:28]2=[CH:32][CH:33]=[CH:34][CH:35]=[C:27]12.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OCC)=O)=NC(OCC)=O>>[F:25][C:2]([F:1])([F:24])[C:3]1[CH:4]=[CH:5][C:6]([N:17]2[CH:21]=[CH:20][N:19]=[C:18]2[CH2:22][N:30]2[C:26](=[O:36])[C:27]3=[CH:35][CH:34]=[CH:33][CH:32]=[C:28]3[C:29]2=[O:31])=[C:7]([CH:16]=1)[C:8]([C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1)=[O:9]Participants
5
Procedure
In the manner given in Example 17, 5-(trifluoromethyl)-2-[2-(hydroxymethyl)imidazol-1-yl]benzophenone is treated with phthalimide and triphenylphosphine and finally with diethyl azocarboxylate to give 5-(trifluoromethyl)-2-[2-(phthalimidomethyl)imidazol-1-yl]benzophenone.
Sources & evidence
- ORD record
- ord-253b5ea5c786489083a0dafc8e118ee2
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03941803
Reaction notes
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