Ethanol → Ethyl 4-(3-methyl-4'-nitro-1,1'-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate

Temperatur

50 °C

A mixture of diethyl 2-[2-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)-2-oxoethyl]-2-(2-phenylethyl)malonate (4.87 g, 9.41 mmol), 1 N aqueous sodium hydroxide (10.4 mL, 10.40 mmol), ethanol (10 mL), and acetone (10 mL) was stirred at 50° C. overnight. The mixture was concentrated and the residue was dissolved in dimethoxyethane (20 mL), and stirred at 80° C. overnight. The mixture was concentrated, and the residue was dissolved in ethyl acetate (30 mL). The solution was washed with water (2×5 mL), dried over magnesium sulfate, and concentrated under reduced pressure. The material obtained was purified by flash chromatography (10:90 ethyl acetate/hexane) to give ethyl 4-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)-4-oxo-2-(2-phenylethyl)butanoate as a light yellow oil (3.53 g, 99% yield). LC-MS ret. time 4.18 min, m/z 446.0 (MH+); 1H NMR (CDCl3) δ: 1.33 (t, 3H), 1.83–2.17 (m, 2H), 2.58 (s, 3H), 2.67–2.78 (m, 2H), 3.00 (dd, 1H), 3.14 (m, 1H), 3.49 (dd, 1H), 4.09 (q, 2H), 7.14–7.36 (m, 5H), 7.47–7.55 (m, 2H), 7.72–7.83 (m, 3H), 8.33 (d, 2H).

1. concentrationThe mixture was concentrated
2. dissolutionthe residue was dissolved in dimethoxyethane (20 mL)
3. stirringstirred at 80° C. overnight
4. concentrationThe mixture was concentrated
5. dissolutionthe residue was dissolved in ethyl acetate (30 mL)
6. washThe solution was washed with water (2×5 mL)
7. dry with materialdried over magnesium sulfate
8. concentrationconcentrated under reduced pressure
9. customThe material obtained
10. customwas purified by flash chromatography (10:90 ethyl acetate/hexane)

ORD-Eintrag

ord-dc5c41d608fa4163b1a900774a6d08b6

Quelldatensatz

uspto-grants-2006_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07091228B2