Реакция #1382677
ord-b0a43e8d8ef34da0b1026e8a6c36f9e3
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1ЭкстракцияThe di-aldehyde was extracted with DCE (2×15 mL)
- 2Промывкаwashed with water (5×10 mL
- 3Другоеuntil no reaction to starch iodide
- 4Промывкаaqueous wash),
- 5ДругоеThe solvent was removed in vacuo
- 6Другоеthe residue was quenched with saturated aqueous NaHCO3 solution
- 7ЭкстракцияThe product was extracted with EtOAc (3×30 mL)
- 8Промывкаwashed with saturated aqueous NaCl solution (1×30 mL)
- 9Сушкаdried over Na2SO4
- 10Фильтрацияfiltered through a silica pad (2×3 in)
- 11Промывкаeluted with 100% EtOAc
- 12Концентрированиеconcentrated
Методика
1,4,5,6-Tetrachloro-7,7-dimethoxy-bicyclo[2.2.1]hept-5-ene-2,3-diol (1.23 g, 3.80 mmol) and sodium periodate (1.19 g, 3.80 mmol) were stirred vigorously for 1.5 h in DCE (10 mL) and water (10 mL). The di-aldehyde was extracted with DCE (2×15 mL), washed with water (5×10 mL, or until no reaction to starch iodide is observed in the aqueous wash), then filtered through a cotton plug under N2 into a slurry of p-methoxybenzylamine (0.52 mL, 3.99 mmol) and NaBH(OAc)3 (2.58 g, 12.16 mmol) in DCE (10 mL). After 3 h at room temperature the reaction was judged complete by TLC. The solvent was removed in vacuo, and the residue was quenched with saturated aqueous NaHCO3 solution. The product was extracted with EtOAc (3×30 mL), washed with saturated aqueous NaCl solution (1×30 mL), dried over Na2SO4, filtered through a silica pad (2×3 in), eluted with 100% EtOAc and concentrated to yield the title compound as a white solid (1.32 g, 82%). (TLC 30% EtOAc/hexanes Rf 0.65); 1H NMR (400 MHz, CDCl3) δ 7.12 (d, J=8.3 Hz, 2H), 6.81 (d, J=8.3 Hz, 2H), 3.77 (s, 3H), 3.61 (s, 2H), 3.59 (s, 3H), 3.56 (s, 3H), 2.76 (d, J=11.4 Hz, 2H), 2.71 (d, J=11.1 Hz, 2H); GCMS m/z 427 (M)+.