Реакция #9334
ord-bb3f18366ce74ecf87b393633f01ba46
Уравнение реакции
9-1
(Z)-7-[(1R,2S,3R,5R)-3-(tert-Butyl-dimethyl-silanyloxy)-5-chloro-2-(4-hydroxymethyl-phenyl)-cyclopentyl]-hept-5-enoic acid methyl ester
NMO
→
9-2
Выход 79.7%
(Z)-7-[(1R,2S,3R,5R)-3-(tert-Butyl-dimethyl-silanyloxy)-5-chloro-2-(4-formyl-phenyl)-cyclopentyl]-hept-5-enoic acid methyl ester
Выход 79.7%
Реактанты
Реагенты
Растворители
Условия реакции
Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1workup.WAITfor 1 h at room temperature
- 2ФильтрацияThe mixture was then filtered through a pad of silica gel
- 3Промывкаwashing with ethyl acetate
- 4ДругоеThe solvents were evaporated
- 5Другоеthe residue was purified by flash chromatography on silica gel (10% ethyl acetate/hexanes)
Методика
An ice cold mixture of 9-1 (43 mg, 0.089 mmol), 4 Å molecular sieves (56 mg) and NMO (16 mg, 0.14 mmol) in dichloromethane (0.5 mL) was treated with TPAP (3 mg, 0.009 mmol). The mixture was stirred for 5 min. at 0° C. and then for 1 h at room temperature. The mixture was then filtered through a pad of silica gel, washing with ethyl acetate. The solvents were evaporated and the residue was purified by flash chromatography on silica gel (10% ethyl acetate/hexanes) to give 9-2 (34 mg, 79%).