4-Toluenesulfonyl chloride → HCID 18789480, compound
Reaction equation
[OH:1][CH2:2][CH2:3][CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][N:5]1[C:10]([O:12][CH2:13][CH2:14][CH2:15][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][CH3:30])=[O:11].[C:31]1([CH3:41])[CH:36]=[CH:35][C:34]([S:37](Cl)(=[O:39])=[O:38])=[CH:33][CH:32]=1.[OH-].[Na+]>O1CCOCC1>[S:37]([O:1][CH2:2][CH2:3][CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][N:5]1[C:10]([O:12][CH2:13][CH2:14][CH2:15][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][CH3:30])=[O:11])([C:34]1[CH:35]=[CH:36][C:31]([CH3:41])=[CH:32][CH:33]=1)(=[O:39])=[O:38]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1,4-Dioxane solution of octadecyl 2-(2-hydroxyethyl)piperidinecarboxylate and p-toluenesulfonyl chloride is added to sodium hydroxide solution and the mixture is reacted at room temperature to obtain octadecyl 2-[2-(tosyloxy)ethyl]piperidinecarboxylate.
Workup
- customthe mixture is reacted at room temperature
Sources & evidence
- ORD record
- ord-d966ab9d6c6148f9ad259a7d72c92e3f
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06057337
Reaction notes
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