HCID 10261278, compound → HCID 21645454, compound

HRID 1493411Notes

Reaction equation

HRID 1493411 reaction equation
[OH:1][CH:2]1[CH2:7][C:6]([CH3:9])([CH3:8])[N:5]([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[C:4]([CH3:20])([CH3:19])[CH2:3]1.Cl[P:22]1[N:26]([CH3:27])[CH2:25][CH2:24][N:23]1[CH3:28]>>[CH3:28][N:23]1[CH2:24][CH2:25][N:26]([CH3:27])[P:22]1[O:1][CH:2]1[CH2:7][C:6]([CH3:8])([CH3:9])[N:5]([O:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])[C:4]([CH3:19])([CH3:20])[CH2:3]1

Participants

3

Reactant 2

HCID 10261278HCID 10261278, compoundHCID 113466831-Octyloxy-2,2,6,6-tetramethylpiperidin-4-ol

Product 1

HCID 21645454HCID 21645454, compound

Procedure

The title compound is prepared from 4-hydroxy-1-octyloxy-2, 2,6,6-tetramethylpiperidine and 2-chloro-1,3-dimethyl-1,3,2-diazaphospholidine according to the procedure of Example 6.

Sources & evidence

ORD record
ord-192bfbfba6c343e597f6cf62a276f508
Source dataset
uspto-grants-1991_06
Patent number
US05021481

Reaction notes

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