HRID133642

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11635

Octadecane

C18H38

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

HCID326921

Bis(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl) butanedioate

C22H40N2O6

PRODUCTS

生成物

结构：CCCCCCCCCCCCCCCCCCON1C(C)(C)CC(OC(=O)CCC(=O)OC2CC(C)(C)N(OCCCCCCCCCCCCCCCCCC)C(C)(C)C2)CC1(C)C

HCID50943392

未命名化合物

PROCEDURE

实验过程

The title compound is prepared from the reaction of bis(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl) succinate and octadecane following a procedure similar to that of Example 4.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-70fb5fcb0e154e47adf32707ae99477e
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:19][CH:20]1[CH2:25][C:24]([CH3:27])([CH3:26])[N:23]([OH:28])[C:22]([CH3:30])([CH3:29])[CH2:21]1)(=[O:18])[CH2:2][CH2:3][C:4]([O:6][CH:7]1[CH2:12][C:11]([CH3:14])([CH3:13])[N:10]([OH:15])[C:9]([CH3:17])([CH3:16])[CH2:8]1)=[O:5].[CH3:31][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][CH3:48]>>[C:1]([O:19][CH:20]1[CH2:25][C:24]([CH3:27])([CH3:26])[N:23]([O:28][CH2:48][CH2:47][CH2:46][CH2:45][CH2:44][CH2:43][CH2:42][CH2:41][CH2:40][CH2:39][CH2:38][CH2:37][CH2:36][CH2:35][CH2:34][CH2:33][CH2:32][CH3:31])[C:22]([CH3:30])([CH3:29])[CH2:21]1)(=[O:18])[CH2:2][CH2:3][C:4]([O:6][CH:7]1[CH2:12][C:11]([CH3:14])([CH3:13])[N:10]([O:15][CH2:48][CH2:47][CH2:46][CH2:45][CH2:44][CH2:43][CH2:42][CH2:41][CH2:40][CH2:39][CH2:38][CH2:37][CH2:36][CH2:35][CH2:34][CH2:33][CH2:32][CH3:31])[C:9]([CH3:17])([CH3:16])[CH2:8]1)=[O:5]