Azobisisobutyronitrile → HCID 70624875, compound

HRID 2419637Notes

Reaction equation

HRID 2419637 reaction equation
[C:1]([O:11][CH2:12][C:13]([O:15][CH:16]=[CH2:17])=[O:14])(=[O:10])[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[C:18]([O:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])(=[O:22])[C:19]([CH3:21])=[CH2:20].N(C(C)(C)C#N)=NC(C)(C)C#N>CC(C)=O>[C:1]([O:11][CH2:12][C:13]([O:15][CH:16]=[CH2:17])=[O:14])(=[O:10])[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[C:18]([O:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])(=[O:22])[C:19]([CH3:21])=[CH2:20]

Participants

5

Procedure

2 g of vinyloxycarbonylmethyl cinnamate prepared according to Example 1 are copolymerized with 1 g of stearyl methacrylate in solution in 2 g of acetone, in the presence of 0.3 g of azobis-isobutyronitrile.

Sources & evidence

ORD record
ord-111f9736905a4de6be0ff39ff3229fe3
Source dataset
uspto-grants-1978_08
Patent number
US04107290

Reaction notes

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