Реакция #2130078

ord-9c5f80d8943d43798ba4812aead649bc

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураto reflux
  2. 2
    ТемператураThe mixture was cooled
  3. 3
    Другоеthe solvent was removed under vacuum
  4. 4
    ДругоеThe residue was partitioned between methylene chloride (100 mL) and water (100 mL)
  5. 5
    ПромывкаThe organic layer was washed with water (2×100 mL)
  6. 6
    Сушкаdried (MgSO4)
  7. 7
    Другоеevaporated under vacuum

Методика

A solution of N-(6-iodobenzo[d][1,3]dioxol-5-yl)acetamide (200 mg, 0.656 mmol) and NaOH (1.31 g, 32.8 mmol) in ethanol (26 mL) and water (6 mL) was heated to reflux with stirring for 4 h. The mixture was cooled and the solvent was removed under vacuum. The residue was partitioned between methylene chloride (100 mL) and water (100 mL). The organic layer was washed with water (2×100 mL), dried (MgSO4) and evaporated under vacuum to give 6-iodobenzo[d][1,3]dioxol-5-amine (170 mg, 98%) as orange solid. LCMS: 264 [M+1]+; 1H NMR (DMSO-d6) δ 4.88 (s, 2H), 5.87 (s, 2H), 6.47 (s, 1H), 7.07 (s, 1H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08586605B2uspto-grants-2013_11