Stearoyl chloride → HCID 20792519, compound

HRID 900411Notes

Reaction equation

HRID 900411 reaction equation
[CH2:1]([C:3]1([CH3:14])[CH:8]([CH3:9])[CH2:7][CH2:6][C:5]([CH2:11][CH3:12])([CH3:10])[NH+:4]1[O-:13])[CH3:2].[C:15](Cl)(=[O:33])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32].C(ON1C(CC)(C)CCC(C)C1(CC)C)(=O)C>>[C:15]([O:13][N:4]1[C:5]([CH2:11][CH3:12])([CH3:10])[CH2:6][CH2:7][CH:8]([CH3:9])[C:3]1([CH2:1][CH3:2])[CH3:14])(=[O:33])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]

Participants

4

Reactant 3

HCID 8212Stearoyl chlorideHCID 20792518HCID 20792518, compoundHCID 22182254HCID 22182254, compound

Product 1

HCID 20792519HCID 20792519, compound

Procedure

2,6-Diethyl-2,3,6-trimethylpiperidine 1-oxide (for preparation, see U.S. Pat. No. 4,131,599) is converted by a method analogous to Example A 30 using stearoyl chloride into the compound 137 which is obtained in the form of a colourless oil.

Workup

  1. customis obtained in the form of a colourless oil

Sources & evidence

ORD record
ord-31117a44d4fd45a0b317be0744a5dd26
Source dataset
uspto-grants-2008_04
Patent number
US07358365B2

Reaction notes

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