HRID1493405

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：CCCCCCCCCCCCNC1CC(C)(C)N(OC2CCCCC2)C(C)(C)C1

HCID19768347

未命名化合物

PRODUCTS

生成物

结构：CCCCCCCCCCCCN(C1CC(C)(C)N(OC2CCCCC2)C(C)(C)C1)P1OCC2(CO1)COP(N(CCCCCCCCCCCC)C1CC(C)(C)N(OC3CCCCC3)C(C)(C)C1)OC2

HCID57679226

未命名化合物

PROCEDURE

实验过程

The title compound is prepared as a viscous oil from 1-cyclohexyloxy-4-dodecylamino-2,2,6,6-tetramethylpiperidine (made in Example 12A) 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-c99a232d51e24740aef5efe044841112
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][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH2:10][C:9]2([CH3:30])[CH3:29])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl[P:32]1[O:37][CH2:36][C:35]2([CH2:42][O:41][P:40](Cl)[O:39][CH2:38]2)[CH2:34][O:33]1>>[CH:1]1([O:7][N:8]2[C:9]([CH3:29])([CH3:30])[CH2:10][CH:11]([N:16]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[P:32]3[O:37][CH2:36][C:35]4([CH2:42][O:41][P:40]([N:16]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH:11]5[CH2:12][C:13]([CH3:14])([CH3:15])[N:8]([O:7][CH:1]6[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]6)[C:9]([CH3:29])([CH3:30])[CH2:10]5)[O:39][CH2:38]4)[CH2:34][O:33]3)[CH2:12][C:13]2([CH3:14])[CH3:15])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1