Maleimide → HCID 131715433, compound

HRID 2413880Notes

Reaction equation

[C:1]1(=[O:7])[NH:5][C:4](=[O:6])[CH:3]=[CH:2]1.[CH:8]([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])=[CH2:9]>>[C:4]1(=[O:6])[NH:5][C:1](=[O:7])[CH:2]=[CH:3]1.[CH:8]([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])=[CH2:9]

Participants

Reactant 2

HCID 10935Maleimide

HCID 13585Octadecane, 1-(ethenyloxy)-

Product 1

HCID 131715433HCID 131715433, compoundYield 61%

Procedure

A polymer was prepared in the manner of Example 1, except the comonomer to maleimide was n-octadecyl vinyl ether. The polymer yield was 61%.

Sources & evidence

ORD record: ord-7d6bec634ed34c7085ee16390e7e21c9
Source dataset: uspto-grants-1988_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04720445

Reaction notes

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