1,5-bismaleimido-2 methyl pentane → HCID 86639887, compound

HRID 560948Notes

Reaction equation

HRID 560948 reaction equation
[SH:1][CH2:2][CH2:3][C:4]([OH:6])=[O:5].[SH:7][CH2:8][CH2:9][C:10]([OH:12])=[O:11].[SH:13][CH2:14][CH2:15][C:16]([OH:18])=[O:17].[CH2:19]([C:21]([CH2:26][OH:27])([CH2:24][OH:25])[CH2:22][CH3:23])[OH:20].[C:28]1(=[O:47])[N:32]([CH2:33][CH:34]([CH3:45])[CH2:35][CH2:36][CH2:37][N:38]2[C:42](=[O:43])[CH:41]=[CH:40][C:39]2=[O:44])[C:31](=[O:46])[CH:30]=[CH:29]1.[C:48]1(=[O:70])[N:52]([C:53]([CH3:68])([CH3:67])[CH:54]([CH3:66])[CH2:55][CH2:56][CH2:57][CH2:58][N:59]2[C:63](=[O:64])[CH:62]=[CH:61][C:60]2=[O:65])[C:51](=[O:69])[CH:50]=[CH:49]1>>[SH:1][CH2:2][CH2:3][C:4]([OH:6])=[O:5].[SH:7][CH2:8][CH2:9][C:10]([OH:12])=[O:11].[SH:13][CH2:14][CH2:15][C:16]([OH:18])=[O:17].[CH2:19]([C:21]([CH2:26][OH:27])([CH2:24][OH:25])[CH2:22][CH3:23])[OH:20].[C:31]1(=[O:46])[N:32]([CH2:33][CH:34]([CH3:45])[CH2:35][CH2:36][CH2:37][N:38]2[C:39](=[O:44])[CH:40]=[CH:41][C:42]2=[O:43])[C:28](=[O:47])[CH:29]=[CH:30]1.[C:51]1(=[O:69])[N:52]([C:53]([CH3:67])([CH3:68])[CH:54]([CH3:66])[CH2:55][CH2:56][CH2:57][CH2:58][N:59]2[C:60](=[O:65])[CH:61]=[CH:62][C:63]2=[O:64])[C:48](=[O:70])[CH:49]=[CH:50]1

Participants

4

Reactant 3

HCID 45195571,5-bismaleimido-2 methyl pentaneHCID 19750998HCID 19750998, compoundHCID 71317278HCID 71317278, compound

Product 1

HCID 86639887HCID 86639887, compound

Procedure

An exemplary formulation was prepared containing trimethylolpropane tri(3-mercaptopropionate) (47%), 1,5-bismaleimido-2 methyl pentane (compound C-2; 24%), 1,6-bismaleimido-trimethyl hexane (compound C-1; 28%), Ancamine 2337S (1%). The formulation was oven-cured at 80° C. for 30 minutes. The die shear data obtained are summarized in Table 2, below.

Workup

  1. customAn exemplary formulation was prepared
  2. customThe die shear data obtained

Sources & evidence

ORD record
ord-de896e906d894de2903a3f1bb18798c1
Source dataset
uspto-grants-2011_11
Patent number
US08063161B2

Reaction notes

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