Sulfuric Acid → HCID 18371959, compound

HRID 1383252Notes

Reaction equation

HRID 1383252 reaction equation
[OH:1][N:2]1[C:7]([CH3:9])([CH3:8])[CH2:6][CH:5]([OH:10])[CH2:4][C:3]1([CH3:12])[CH3:11].[S:13](=[O:17])(=[O:16])([OH:15])[OH:14]>O>[S:13]([O-:17])([O-:16])(=[O:15])=[O:14].[OH:1][NH+:2]1[C:7]([CH3:8])([CH3:9])[CH2:6][CH:5]([OH:10])[CH2:4][C:3]1([CH3:12])[CH3:11].[OH:1][NH+:2]1[C:7]([CH3:8])([CH3:9])[CH2:6][CH:5]([OH:10])[CH2:4][C:3]1([CH3:12])[CH3:11]

Participants

4

Procedure

To a glass 0.5L reaction bottle are added 10.0 g (58 mmol) of 1-oxyl-2,2,6,6-tetramethyl-4-hydroxypiperidine, 2.85g (29 mmol) sulfuric acid, 200 mg 5% Pt on C and 100 mL water. Catalytic hydrogenation is carried out at 50 psi for 30 minutes at room temperature. Catalyst is removed by filtration through a pad of Celite. Removal of water yields the product as an pale yellow solid.

Workup

  1. customCatalyst is removed by filtration through a pad of Celite
  2. customRemoval of water

Sources & evidence

ORD record
ord-76b363e594564a2d8c67cb9104848a40
Source dataset
uspto-grants-2001_07
Patent number
US06254724B1

Reaction notes

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