HRID224683

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID6547

Azobisisobutyronitrile

C8H12N4

HCID122600

Stearyl methacrylate

C22H42O2

HCID54571820

未命名化合物

HCID178514658

未命名化合物

PRODUCTS

生成物

结构：C=C(C)C(=O)OCCCCCCCCCCCCCCCCCC.C=CC(=O)NCc1cc(O)ccc1C(=O)c1ccccc1

HCID86733966

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID180

Acetone

C3H6O

CONDITIONS

反应条件

温度: 80 °C

PROCEDURE

实验过程

Into a 50 ml flask provided with a condenser, a nitrogen lead in tube and an agitator, there are intorduced 1 g of acrylamido methyl 4-hydroxy benzophenone, 1.5 g of stearyl methacrylate and 0.25 g of azobis-isobutyronitrile in solution in 5 ml of acetone. The resulting mixture is heated for 8 hours at 80° C.

WORKUP

后处理

customInto a 50 ml flask provided with a condenser

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-f12a8b52012e49d5a2ccfc21ae104854
来源数据集: uspto-grants-1980_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04233430
来源说明: uspto-grants-1980_11

反应 SMILES

[Pb].[N].[C:3]([NH:7][CH2:8][C:9]1[CH:22]=[C:21]([OH:23])[CH:20]=[CH:19][C:10]=1[C:11]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:12])(=[O:6])[CH:4]=[CH2:5].[C:24]([O:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH3:47])(=[O:28])[C:25]([CH3:27])=[CH2:26].N(C(C)(C)C#N)=NC(C)(C)C#N>CC(C)=O>[C:3]([NH:7][CH2:8][C:9]1[CH:22]=[C:21]([OH:23])[CH:20]=[CH:19][C:10]=1[C:11]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:12])(=[O:6])[CH:4]=[CH2:5].[C:24]([O:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH3:47])(=[O:28])[C:25]([CH3:27])=[CH2:26]