Ethanesulfonyl chloride → 8-(Ethylsulfonylamino)octanoic acid

HRID 605496노트

반응식

HRID 605496 반응식
[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]

참가 물질

5

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-ae31607607244fe2b8f8e2d80d12d7f8
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07915236B2

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