HRID364251

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID17318

3-(Trimethoxysilyl)propyl methacrylate

C10H20O5Si

HCID116807

1-Disiloxanol, 1,1,3,3,3-pentamethyl-, 1-acetate

C7H18O3Si2

结构：CC(=O)O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](OC(C)=O)(O[Si](C)(C)C)O[Si](C)(C)C

HCID20240556

未命名化合物

PRODUCTS

生成物

结构：C=C(C)C(=O)OCCC[Si](O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](CCCOC(=O)C(=C)C)([Si](C)(C)O[Si](C)(C)C)[Si](C)(C)O[Si](C)(C)C)([Si](C)(C)O[Si](C)(C)C)[Si](C)(C)O[Si](C)(C)C

HCID21242010

未命名化合物

PROCEDURE

实验过程

This monomer was prepared in a manner similar to that described in Example 1. The reactants were γ-methacryloxypropyltrimethoxysilane (2 moles), 1,3-Bis(acetoxy)-1,1,3,3-TETRA(trimethylsiloxy)disiloxane (1 mole) and acetoxypentamethyldisiloxane (4 moles). This material is designated SM-16.

WORKUP

后处理

customThis monomer was prepared in a manner similar to

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-79948a3809964cda85ea17fda0a7b043
来源数据集: uspto-grants-1986_08
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04604479
来源说明: uspto-grants-1986_08

反应 SMILES

[C:1]([O:6][CH2:7][CH2:8][CH2:9][Si:10](OC)(OC)OC)(=[O:5])[C:2]([CH3:4])=[CH2:3].C([O:20][Si:21]([O:43][Si:44]([CH3:47])([CH3:46])[CH3:45])([O:38][Si:39]([CH3:42])([CH3:41])[CH3:40])[O:22][Si:23]([O:34]C(=O)C)([O:29][Si:30]([CH3:33])([CH3:32])[CH3:31])O[Si](C)(C)C)(=O)C.C(O[Si:52]([CH3:59])([CH3:58])[O:53][Si:54]([CH3:57])([CH3:56])[CH3:55])(=O)C>>[C:1]([O:6][CH2:7][CH2:8][CH2:9][Si:10]([Si:52]([CH3:58])([CH3:59])[O:53][Si:54]([CH3:55])([CH3:56])[CH3:57])([Si:52]([CH3:59])([CH3:58])[O:53][Si:54]([CH3:57])([CH3:56])[CH3:55])[O:34][Si:23]([O:29][Si:30]([CH3:33])([CH3:32])[CH3:31])([O:29][Si:30]([CH3:31])([CH3:32])[CH3:33])[O:22][Si:21]([O:38][Si:39]([CH3:40])([CH3:41])[CH3:42])([O:43][Si:44]([CH3:45])([CH3:46])[CH3:47])[O:20][Si:10]([CH2:9][CH2:8][CH2:7][O:6][C:1](=[O:5])[C:2]([CH3:4])=[CH2:3])([Si:52]([CH3:59])([CH3:58])[O:53][Si:54]([CH3:57])([CH3:56])[CH3:55])[Si:52]([CH3:59])([CH3:58])[O:53][Si:54]([CH3:57])([CH3:56])[CH3:55])(=[O:5])[C:2]([CH3:4])=[CH2:3]