Реакция #1563900

ord-16c44bf04bb44c7fb669217a3f527209

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураat refluxed temperature
  2. 2
    Фильтрацияthe mixture was filtered
  3. 3
    Промывкаwashed with methanol
  4. 4
    КонцентрированиеThe filtrate was concentrated
  5. 5
    Другоеpurified by column chromatography (petroleum ether/ethyl acetate 1%-5%)

Методика

The above prepared 5-tert-Butyl-6-nitrobenzo[d][1,3]dioxole (1.1 g, 5 mmol), Fe (5.5 g, 100 mmol) and HCl (2 ml) was added into ethanol (6 ml) and water (18 ml). The mixture was stirred for 2 h at refluxed temperature. The PH was adjusted to 7-8 and the mixture was filtered and washed with methanol. The filtrate was concentrated and purified by column chromatography (petroleum ether/ethyl acetate 1%-5%) to give 6-tert-butylbenzo[d][1,3]dioxol-5-amine (240 mg, 25%) as a red solid. LCMS: 194 [M+1]+; 1H NMR (400M): (DMSO-d6) δ 1.28 (s, 9H), 4.46 (s, 2H), 5.77 (s, 2H), 6.32 (s, 1H), 6.63 (s, 1H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09402832B2uspto-grants-2016_08