Phthalimide → HCID 21555829, compound

HRID 267444Notes

Reaction equation

HRID 267444 reaction equation
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([N:18]2[CH:22]=[CH:21][N:20]=[C:19]2[CH2:23]O)=[C:8]([CH:17]=1)[C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:10])([O-:3])=[O:2].[C:25]1(=[O:35])[NH:29][C:28](=[O:30])[C:27]2=[CH:31][CH:32]=[CH:33][CH:34]=[C:26]12.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OCC)=O)=NC(OCC)=O>>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([N:18]2[CH:22]=[CH:21][N:20]=[C:19]2[CH2:23][N:29]2[C:25](=[O:35])[C:26]3=[CH:34][CH:33]=[CH:32][CH:31]=[C:27]3[C:28]2=[O:30])=[C:8]([CH:17]=1)[C:9]([C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)=[O:10])([O-:3])=[O:2]

Participants

5

Reactant 4

HCID 6809PhthalimideHCID 11776TriphenylphosphineHCID 220568ethyl N-ethoxycarbonyliminocarbamateHCID 13179829HCID 13179829, compound

Product 1

HCID 21555829HCID 21555829, compound

Procedure

In the manner given in Example 17, 5-nitro-2-[2-(hydroxymethyl)imidazol-1-yl]benzophenone is treated with phthalimide and triphenylphosphine and finally with diethyl azodicarboxylate to give 5-nitro-2-[2-(phthalimidomethyl)imidazol-1-yl]benzophenone.

Sources & evidence

ORD record
ord-a5ad2dc0293e4cb5bfbe719a043ec277
Source dataset
uspto-grants-1976_03
Patent number
US03941803

Reaction notes

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