Реакция #1833234

ord-ced94af8c2b14187a517a5cd2b9b1adf

Уравнение реакции

C[O-].[Na+]
sodium methoxide
O=[N+]([O-])c1cc2c(cc1F)OC(F)(F)O2
2,2,5-Trifluoro-6-nitrobenzo[d][1,3]dioxole
C[O-]
methoxide
CC(=O)O
acetic acid
COc1cc2c(cc1[N+](=O)[O-])OC(F)(F)O2
title compound
Выход 70.0%
COc1cc2c(cc1[N+](=O)[O-])OC(F)(F)O2
2,2-Difluoro-5-methoxy-6-nitrobenzo[d][1,3]dioxole
Выход 70.0%

Растворители

Условия реакции

Температура
20°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe volatiles were removed by rotary evaporation
  2. 2
    Промывкаwashed with saturated NaHCO3 (10 mL), saturated NaCl (10 mL)
  3. 3
    Сушкаdried (Na2SO4)
  4. 4
    Другоеevaporated
  5. 5
    ДругоеThe material was purified by chromatography on silica with a 0-30% ethyl acetate-hexane gradient

Методика

2,2,5-Trifluoro-6-nitrobenzo[d][1,3]dioxole (2.5 g, 11 mmol) was dissolved in dry methanol (20 mL), treated with 30% sodium methoxide solution (3.1 g, 17 mmol), and stirred at 20° C. for 1 h. After excess methoxide was neutralized by addition of acetic acid, the volatiles were removed by rotary evaporation. The residue was taken up in ethyl acetate (50 mL), washed with saturated NaHCO3 (10 mL), saturated NaCl (10 mL), dried (Na2SO4) and evaporated. The material was purified by chromatography on silica with a 0-30% ethyl acetate-hexane gradient to give the title compound as a white solid (1.8 g, 70%): mp 84-85° C. 1H NMR (400 MHz, CDCl3) δ 7.71 (s, 1H), 6.89 (s, 1H), 3.98 (s, 3H); 19F NMR (376 MHz, CDCl3) δ −49.90 (s); EIMS m/z 233.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09149038B2uspto-grants-2015_10