HRID224684

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID6547

Azobisisobutyronitrile

C8H12N4

HCID122600

Stearyl methacrylate

C22H42O2

结构：C=CC(=O)NCc1c(OC)ccc(C(=O)c2ccccc2)c1O

HCID86733968

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)NCc1c(OC)ccc(C(=O)c2ccccc2)c1O

HCID86733967

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID180

Acetone

C3H6O

PROCEDURE

实验过程

Into a 50 ml flask provided with a condenser, a nitrogen lead in tube and an agitator, there are introduced 2.5 g of acrylamido methyl-4-methoxy-2-hydroxy benzophenone, 2.5 g of stearyl methacrylate and 0.2 g of azobis-isobutyronitrile in solution in 10 g of acetone.

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-d06f45e63f1d45a19e1f9cb161c250d3
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[C:10]([OH:25])=[C:11]([CH:20]=[CH:21][C:22]=1[O:23][CH3:24])[C:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:13])(=[O:6])[CH:4]=[CH2:5].[C:26]([O: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][CH2:47][CH2:48][CH3:49])(=[O:30])[C:27]([CH3:29])=[CH2:28].N(C(C)(C)C#N)=NC(C)(C)C#N>CC(C)=O>[C:3]([NH:7][CH2:8][C:9]1[C:10]([OH:25])=[C:11]([CH:20]=[CH:21][C:22]=1[O:23][CH3:24])[C:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:13])(=[O:6])[CH:4]=[CH2:5].[C:26]([O: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][CH2:47][CH2:48][CH3:49])(=[O:30])[C:27]([CH3:29])=[CH2:28]