Dodecylamine → HCID 19768347, compound

HRID 1493401Notes

Reaction equation

HRID 1493401 reaction equation
[CH:1]1([O:7][N:8]2[C:13]([CH3:15])([CH3:14])[CH2:12][C:11](=O)[CH2:10][C:9]2([CH3:18])[CH3:17])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:19]([NH2:31])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30]>>[CH:1]1([O:7][N:8]2[C:13]([CH3:15])([CH3:14])[CH2:12][CH:11]([NH:31][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[CH2:10][C:9]2([CH3:18])[CH3:17])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

3

Reactant 2

HCID 13583DodecylamineHCID 22019868N-cyclohexyloxy-4-oxo-2,2,6,6-tetramethylpiperidine

Product 1

HCID 19768347HCID 19768347, compoundYield 82%

Procedure

The title compound is prepared in 82% yield as a colorless syrup from 1-cyclohexyloxy-2,2,6,6,-tetramethyl-piperidin-4-one and dodecylamine according to the procedure of Example 11B.

Sources & evidence

ORD record
ord-0e0c690b73b84564b26ace455a2338b1
Source dataset
uspto-grants-1991_06
Patent number
US05021481

Reaction notes

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