Ethanesulfonyl chloride → 8-(Ethylsulfonylamino)octanoic acid
Reaction equation
[CH2:1]([S:3](Cl)(=[O:5])=[O:4])[CH3:2].[NH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]([OH:17])=[O:16]>O1CCOCC1.[OH-].[Na+]>[CH2:1]([S:3]([NH:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]([OH:17])=[O:16])(=[O:5])=[O:4])[CH3:2]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of ethanesulfonyl chloride (1.5 ml, 15.7 mmol) in dioxane (5 ml) was added to a solution of 8-aminooctanoic acid (1 g, 6.28 mmol) in 1N NaOH (22 ml) and dioxane (5 ml), while stirring at 0° C.-5° C. The mixture was allowed to warm to room temperature and stirred for 3.5 minutes. During this period, at 1 hour intervals, the pH was adjusted to 7-8 by addition of 25% NaOH solution. The reaction mixture was washed with diethyl ether (30 ml). The pH was adjusted to 1-2 by addition of 1N HCl and the mixture was extracted with ethyl acetate (70 ml). The organic layer was dried over sodium sulfate and concentrated. The residue was triturated with a mixture of diethyl ether. The solid was collected by filtration and dried under vacuum affording 600 mg of the title compound (38% yield).
Workup
- stirringstirred for 3.5 minutes
- waitDuring this period
- washThe reaction mixture was washed with diethyl ether (30 ml)
- additionThe pH was adjusted to 1-2 by addition of 1N HCl
- extractionthe mixture was extracted with ethyl acetate (70 ml)
- dry with materialThe organic layer was dried over sodium sulfate
- concentrationconcentrated
- customThe residue was triturated with a mixture of diethyl ether
- filtrationThe solid was collected by filtration
- customdried under vacuum
Sources & evidence
- ORD record
- ord-b4baf329c40f4b1f964992a85f5da5e1
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07576206B2
Reaction notes
Loading…