N,N'-2-Phenylenedimaleimide → HCID 19834299, compound

HRID 2051079Notes

Reaction equation

HRID 2051079 reaction equation
[C:1]1([N:14]2[C:18](=[O:19])[CH:17]=[CH:16][C:15]2=[O:20])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[N:7]1[C:11](=[O:12])[CH:10]=[CH:9][C:8]1=[O:13].[C:21]([O:29][CH:30]1[CH2:35][C:34]([CH3:37])([CH3:36])[N:33]([OH:38])[C:32]([CH3:40])([CH3:39])[CH2:31]1)(=[O:28])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>>[C:21]([O:29][CH:30]1[CH2:31][C:32]([CH3:40])([CH3:39])[N:33]([O:38][CH:10]2[C:11](=[O:12])[N:7]([C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][C:1]=3[N:14]3[C:18](=[O:19])[CH:17]([O:38][N:33]4[C:34]([CH3:37])([CH3:36])[CH2:35][CH:30]([O:29][C:21](=[O:28])[C:22]5[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=5)[CH2:31][C:32]4([CH3:40])[CH3:39])[CH2:16][C:15]3=[O:20])[C:8](=[O:13])[CH2:9]2)[C:34]([CH3:36])([CH3:37])[CH2:35]1)(=[O:28])[C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1

Participants

3

Reactant 2

HCID 83156N,N'-2-PhenylenedimaleimideHCID 6881781-Hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine

Product 1

HCID 19834299HCID 19834299, compound

Procedure

The title compound is prepared from N,N'-1,2-phenylenedimaleimide and 4-benzoyloxy-1-hydroxy-2,2,6,6-tetramethylpiperidine according to the general procedure of Example 6.

Sources & evidence

ORD record
ord-fcfac193ac084d28a309e9fbfd77f412
Source dataset
uspto-grants-1991_05
Patent number
US05015678

Reaction notes

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