4-Toluenesulfonyl chloride → HCID 18789426, compound
Reaction equation
[CH2:1]([N:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH:20]1[CH2:25][CH2:26][OH:27])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[C:28]1([CH3:38])[CH:33]=[CH:32][C:31]([S:34](Cl)(=[O:36])=[O:35])=[CH:30][CH:29]=1.[OH-].[Na+]>O1CCOCC1>[CH2:1]([N:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH:20]1[CH2:25][CH2:26][O:27][S:34]([C:31]1[CH:32]=[CH:33][C:28]([CH3:38])=[CH:29][CH:30]=1)(=[O:36])=[O:35])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1,4-Dioxane solution of 2-(1-octadecyl-2-piperidyl)ethan-1-ol and p-toluenesulfonyl chloride is added to sodium hydroxide solution and then the mixture is reacted at room temperature to obtain 1-octadecyl-2-[2-(tosyloxy)ethyl]piperidine.
Workup
- customthe mixture is reacted at room temperature
Sources & evidence
- ORD record
- ord-8021140bedfd42f28dc9032336d13f9f
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06057337
Reaction notes
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