Ethanesulfonyl chloride → 8-(Ethylsulfonylamino)octanoic acid

HRID 2103985Notes

Reaction equation

HRID 2103985 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

5

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

  1. stirringstirred for 3.5 minutes
  2. waitDuring this period
  3. washThe reaction mixture was washed with diethyl ether (30 ml)
  4. additionThe pH was adjusted to 1-2 by addition of 1N HCl
  5. extractionthe mixture was extracted with ethyl acetate (70 ml)
  6. dry with materialThe organic layer was dried over sodium sulfate
  7. concentrationconcentrated
  8. customThe residue was triturated with a mixture of diethyl ether
  9. filtrationThe solid was collected by filtration
  10. customdried under vacuum

Sources & evidence

ORD record
ord-b4baf329c40f4b1f964992a85f5da5e1
Source dataset
uspto-grants-2009_08
Patent number
US07576206B2

Reaction notes

Loading…