Реакция #2175447

ord-f92a6fa6655643c8bfd9e6bd0fde5ddb

Уравнение реакции

[N-]=[N+]=[N-].[Na+]
Sodium azide
Cc1ccc(S(=O)(=O)OCCOCCOS(=O)(=O)c2ccc(C)cc2)cc1
diethyleneglycol ditosylate
O
water
Cc1ccc(S(=O)(=O)OCCOCCN=[N+]=[N-])cc1
7
Выход 16.5%
Cc1ccc(S(=O)(=O)OCCOCCN=[N+]=[N-])cc1
5-azido-3-oxa-pentyl p-toluenesulfonate
Выход 16.5%

Реагенты

Нет

Растворители

Условия реакции

Температура
110°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONThe reaction mixture was poured
  2. 2
    Экстракцияthe product was extracted with ethyl acetate (3×100 mL)
  3. 3
    Промывкаthe collected organic extracts were washed with water (3×100 mL), brine
  4. 4
    Сушкаdried over MgSO4
  5. 5
    ДругоеThe crude product was purified on SiO2 and DCM/MeOH 0-100% gradient as eluant

Методика

Sodium azide (0.47 g, 7.24 mmol) added to a solution of diethyleneglycol ditosylate (3 g, 7.24 mmol) in DMF (30 mL) and the resulting mixture was heated to 110° C. for 5 hours. The reaction mixture was poured into chilled water (125 mL) and the product was extracted with ethyl acetate (3×100 mL), the collected organic extracts were washed with water (3×100 mL), brine and dried over MgSO4. The crude product was purified on SiO2 and DCM/MeOH 0-100% gradient as eluant to yield 0.34 g (16%) of 7 as a colorless oil. 1H NMR (400 MHz, CDCl3): δ 2.45 (s, 3H), 3.16 (t, J=4.8 Hz, 2H), 3.60 (t, J=4.8 Hz, 2H), 3.70 (t, J=4.8 Hz, 2H), 4.17 (t, J=4.8 Hz, 2H), 7.35 (d, J=8 Hz, 2H), 7.81 (d, J=8 Hz, 2H); 13C NMR (100.6 MHz, CDCl3): δ 21.6, 50.6, 68.7, 69.1, 70.2, 128.0, 129.9, 133.0, 144.9; MS ESI (m/z): [M+H]+ calcd. for C11H15N3O4S, 286.08; found 286.1

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08435488B2uspto-grants-2013_05