Reaktion #10831
ord-bfb8c66bff4d48099a2e5ecf4d4ad3f8
Reaktionsgleichung
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1workup.ADDITIONThe reaction mixture was poured into ice
- 2ExtraktionThe aqueous solution was extracted with dichloromethane and isopropyl alcohol (33%, v/v, in dichloromethane)
- 3WaschenThe combined dichloromethane and isopropyl alcohol were washed with brine
- 4Trocknendried over sodium sulfate
- 5Einengenconcentrated
- 6workup.ADDITIONThe aqueous solution was treated with sodium hydroxide to pH 12
- 7Extraktionextracted again with isopropyl alcohol (33%, v/v, in dichloromethane)
- 8Sonstigeto give additional product
- 9SonstigeThe crude product was purified by flash chromatography
- 10WaschenElution with methanol (10%, v/v, in dichloromethane)
Vorschrift
Ex-109E: To a solution of 3-(2,4-dimethoxy-phenyl)-4-isobutyl-4H-[1,2,4]triazole (Ex-109D, 0.78 g, 2.98 mmol) was added dichloromethyl methyl ether (0.4 mL, 4.48 mmol) followed by addition of titanium tetrachloride (1.0M in dichloromethane, 9.0 mL, 9.0 mmol) over 10 min at 0° C. The reaction mixture was allowed to stir at 0° C. for 30 min and ambient temperature overnight. The reaction mixture was poured into ice. The aqueous solution was extracted with dichloromethane and isopropyl alcohol (33%, v/v, in dichloromethane). The combined dichloromethane and isopropyl alcohol were washed with brine, dried over sodium sulfate and concentrated. The aqueous solution was treated with sodium hydroxide to pH 12 and extracted again with isopropyl alcohol (33%, v/v, in dichloromethane) to give additional product. The crude product was purified by flash chromatography. Elution with methanol (10%, v/v, in dichloromethane) afford 5-(4-isobutyl-4H-[1,2,4]triazol-3-yl)-2,4-dimethoxy-benzaldehyde (0.24 g, 28%): 1H NMR (CDCl3) δ 10.30 (s, 1H), 8.17 (s, 1H), 7.90 (s, 1H), 6.51 (s, 1H), 4.00 (s, 3H), 3.87 (s, 3H), 3.58 (d, J=7.2 Hz, 2H), 1.91–1.80 (m, 1H), 0.77 (d, J=6.5 Hz, 6H).