HRID441480

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID3314

Eugenol

C10H12O2

HCID15624

2-Allylphenol

C9H10O

HCID6453038

2-Methylenesuccinic acid, potassium salt

C5H4K2O4

HCID23667354

2-Propenoic acid, 2-methyl-, potassium salt (1:1)

C4H5KO2

PRODUCTS

生成物

HCID74458

Allyl phenyl ether

C9H10O

HCID122600

Stearyl methacrylate

C22H42O2

HCID6453038

2-Methylenesuccinic acid, potassium salt

C5H4K2O4

PROCEDURE

实验过程

The procedure for preparing the copolymer in Example 1 was repeated except that potassium itaconate and o-allylphenol were used in place of potassium methacrylate and 4-allyl-2-methoxyphenol, respectively to obtain a copolymer of stearyl methacrylate, potassium itaconate and O-allyl phenol.

WORKUP

后处理

customThe procedure for preparing the copolymer in Example 1

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-7176d33bc2c440be81b131b925769723
来源数据集: uspto-grants-1977_08
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04040970
来源说明: uspto-grants-1977_08

反应 SMILES

[C:1]([O-:9])(=[O:8])[C:2]([CH2:4][C:5]([O-:7])=[O:6])=[CH2:3].[K+:10].[K+].[CH2:12]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[OH:21])[CH:13]=[CH2:14].[C:22]([O-])(=O)[C:23](C)=[CH2:24].[K+].[CH2:29]([C:32]1[CH:37]=[CH:36][C:35](O)=[C:34](OC)[CH:33]=1)[CH:30]=[CH2:31]>>[C:1]([O:9][CH2:31][CH2:30][CH2:29][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:15][CH2:12][CH2:13][CH3:14])(=[O:8])[C:2]([CH3:4])=[CH2:3].[C:1]([O-:9])(=[O:8])[C:2]([CH2:4][C:5]([O-:7])=[O:6])=[CH2:3].[K+:10].[K+:10].[CH2:24]([O:21][C:16]1[CH:15]=[CH:20][CH:19]=[CH:18][CH:17]=1)[CH:23]=[CH2:22]