2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane, 3,9-dichloro- → HCID 86744824, compound

HRID 1493408Notes

Reaction equation

HRID 1493408 reaction equation
[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

Participants

3

Reactant 2

HCID 772022,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane, 3,9-dichloro-HCID 19831377HCID 19831377, compound

Product 1

HCID 86744824HCID 86744824, compound

Procedure

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.

Sources & evidence

ORD record
ord-1568a2cfceee4841a6ef4d16523a603c
Source dataset
uspto-grants-1991_06
Patent number
US05021481

Reaction notes

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