反应详情

Sodium metal (0.46 g, 0.02 g-atom) is added to MeOH (35 mL) portionwise at rt. When a homogeneous solution is obtained, nitrocyclohexane (12.92 g, 100 mmol) is added, followed by o-phthalaldehyde (8.38 g, 60.0 mmol). The resulting solution is stirred at rt overnight. The solution is brought to pH 2 by adding 1 N H2SO4 and stirred at rt for 60 min. White solids precipitate. The mixture is filtered, and the filtrate, from which an oil separates, is made basic by adding 10% NaOH solution. The solution is concentrated in vacuo to remove the MeOH, and the resulting aqueous solution is extracted twice with Et2O. The combined organic layers are washed once with brine, dried (MgSO4), filtered, and concentrated. After final drying on a vacuum pump, a yellow oil is obtained (17.29 g, 100%). The following data were obtained on a ca. 1:1 mixture of the cis and trans diastereoisomers. 1H NMR (CDCl3) 7.45-7.35 (m, 3), 7.20-7.10 (m, 1), 6.26 and 5.55 (isomer I, 2 d, 1 total, J=2.7, and 2.3 Hz, respectively), 5.98 and 5.38 (isomer II, 2 s, 1 total), 3.59 and 3.36 (isomers I and II, respectively, 2s, 3 total), 2.59 (m, 2), 2.22 (m, 2), 1.95-1.10 (m, 6).

1. customWhen a homogeneous solution is obtained
2. stirringstirred at rt for 60 min
3. filtrationThe mixture is filtered
4. additionby adding 10% NaOH solution
5. concentrationThe solution is concentrated in vacuo
6. customto remove the MeOH
7. extractionthe resulting aqueous solution is extracted twice with Et2O
8. washThe combined organic layers are washed once with brine
9. dry with materialdried (MgSO4)
10. filtrationfiltered
11. concentrationconcentrated
12. customAfter final drying on a vacuum pump
13. customa yellow oil is obtained (17.29 g, 100%)
14. customThe following data were obtained on a ca. 1:1 mixture of the cis and trans diastereoisomers