HRID133640

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID13065

2,2-Diphenylpropane

C15H16

结构：CC1(C)CC(OC(=O)CCCCCCCCC(=O)OC2CC(C)(C)N(O)C(C)(C)C2)CC(C)(C)N1O

HCID11272241

Bis-(tetramethyl hydroxypiperidinyl) sebacate

C28H52N2O6

PRODUCTS

生成物

结构：CC(CON1C(C)(C)CC(OC(=O)CCCCCCCCC(=O)OC2CC(C)(C)N(OCC(C)(c3ccccc3)c3ccccc3)C(C)(C)C2)CC1(C)C)(c1ccccc1)c1ccccc1

HCID50943320

未命名化合物

PROCEDURE

实验过程

Bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-y) sebacate and 2,2-diphenylpropane are reacted following a procedure similar to that of Example 6.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-133a4163c1a447cb83fd9ff17cd69572
来源数据集: uspto-grants-2008_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07390904B2
来源说明: uspto-grants-2008_06

反应 SMILES

[C:1]([O:25][CH:26]1[CH2:31][C:30]([CH3:33])([CH3:32])[N:29]([OH:34])[C:28]([CH3:36])([CH3:35])[CH2:27]1)(=[O:24])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:12][CH:13]1[CH2:18][C:17]([CH3:20])([CH3:19])[N:16]([OH:21])[C:15]([CH3:23])([CH3:22])[CH2:14]1)=[O:11].[C:37]1([C:43]([C:46]2[CH:51]=[CH:50][CH:49]=[CH:48][CH:47]=2)([CH3:45])[CH3:44])[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1>>[C:1]([O:25][CH:26]1[CH2:27][C:28]([CH3:36])([CH3:35])[N:29]([O:34][CH2:45][C:43]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)([C:46]2[CH:51]=[CH:50][CH:49]=[CH:48][CH:47]=2)[CH3:44])[C:30]([CH3:33])([CH3:32])[CH2:31]1)(=[O:24])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([O:12][CH:13]1[CH2:14][C:15]([CH3:22])([CH3:23])[N:16]([O:21][CH2:44][C:43]([C:46]2[CH:47]=[CH:48][CH:49]=[CH:50][CH:51]=2)([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[CH3:45])[C:17]([CH3:19])([CH3:20])[CH2:18]1)=[O:11]