HRID1493408

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID77202

2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane, 3,9-dichloro-

C5H8Cl2O4P2

结构：CC1(C)CC(NC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)CC(C)(C)N1OC1CCCCC1

HCID19831377

未命名化合物

PRODUCTS

生成物

结构：CC1(C)CC(N(C2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)P2OCC3(CO2)COP(N(C2CC(C)(C)N(OC4CCCCC4)C(C)(C)C2)C2CC(C)(C)N(OC4CCCCC4)C(C)(C)C2)OC3)CC(C)(C)N1OC1CCCCC1

HCID86744824

未命名化合物

PROCEDURE

实验过程

The title compound is prepared from bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)amine and 3,9-dichloro-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane according to the procedure of Example 14.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-1568a2cfceee4841a6ef4d16523a603c
来源数据集: uspto-grants-1991_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05021481
来源说明: uspto-grants-1991_06

反应 SMILES

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