Reaktion #1833234

ord-ced94af8c2b14187a517a5cd2b9b1adf

Reaktionsgleichung

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
Ausbeute 70.0%
COc1cc2c(cc1[N+](=O)[O-])OC(F)(F)O2
2,2-Difluoro-5-methoxy-6-nitrobenzo[d][1,3]dioxole
Ausbeute 70.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe volatiles were removed by rotary evaporation
  2. 2
    Waschenwashed with saturated NaHCO3 (10 mL), saturated NaCl (10 mL)
  3. 3
    Trocknendried (Na2SO4)
  4. 4
    Sonstigeevaporated
  5. 5
    SonstigeThe material was purified by chromatography on silica with a 0-30% ethyl acetate-hexane gradient

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09149038B2uspto-grants-2015_10