1,3,2-Dioxaphosphorinane, 2-chloro-5,5-dimethyl- → HCID 53919599, compound

HRID 1493409Notes

Reaction equation

HRID 1493409 reaction equation
[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][NH:23][CH:24]3[CH2:29][C:28]([CH3:31])([CH3:30])[N:27]([O:32][CH:33]4[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]4)[C:26]([CH3:40])([CH3:39])[CH2:25]3)[CH2:10][C:9]2([CH3:42])[CH3:41])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl[P:44]1[O:49][CH2:48][C:47]([CH3:51])([CH3:50])[CH2:46][O:45]1>>[CH3:50][C:47]1([CH3:51])[CH2:48][O:49][P:44]([N:23]([CH:24]2[CH2:25][C:26]([CH3:40])([CH3:39])[N:27]([O:32][CH:33]3[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]3)[C:28]([CH3:30])([CH3:31])[CH2:29]2)[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][N:16]([P:44]2[O:49][CH2:48][C:47]([CH3:51])([CH3:50])[CH2:46][O:45]2)[CH:11]2[CH2:12][C:13]([CH3:15])([CH3:14])[N:8]([O:7][CH:1]3[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]3)[C:9]([CH3:42])([CH3:41])[CH2:10]2)[O:45][CH2:46]1

Participants

3

Reactant 2

HCID 755081,3,2-Dioxaphosphorinane, 2-chloro-5,5-dimethyl-HCID 21182128HCID 21182128, compound

Product 1

HCID 53919599HCID 53919599, compound

Procedure

The title compound is prepared from N,N'-bis(1-cyclohexyloxy-2, 2,6,6-tetramethylpiperidin-4-yl)hexamethylenediamine and 2-chloro-5,5-dimethyl-1,3,2-dioxaphosphorinane according to the procedure of Example 11C.

Sources & evidence

ORD record
ord-78858d4813fe4ccf9ecf042a3365e6c4
Source dataset
uspto-grants-1991_06
Patent number
US05021481

Reaction notes

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