Реакция #2644
ord-e0e346db372f42efa4e13b85899186f1
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.STIRRINGis stirred for 30 minutes
- 2Фильтрацияtert-butyl methyl ether (10 mL) and filtered
- 3ДругоеThe phases of the filtrate are separated
- 4Экстракцияthe aqueous phase is extracted with tert-butyl methyl ether (15 mL)
- 5Сушкаdried over magnesium sulfate
- 6Фильтрацияfiltered
- 7Концентрированиеconcentrated under vacuum
- 8ДругоеThe residue is purified by chromatography (silica gel, 30 g, 33% ethyl acetate/hexane)
Методика
A slurry of lithium aluminum hydride (55 mg, 1.44 mmol), lithium iodide (1.65 g, 5.76 mmol), tert-butyl methyl ether (2 mL) and toluene (3 mL) is cooled to -15° C. The slurry is treated dropwise with 4-tert-butoxy-cyclopent-2-enone(430 mg, 2.79 mmol, dissolved in 1 mL of toluene) over 5 minutes. The reaction mixture is stirred at -20° C. to -12° C. for 2 hours and then allowed to warm to room temperature and is stirred for 30 minutes. The reaction mixture is then treated sequentially with sodium hydroxide (1N, 1 mL), then tert-butyl methyl ether (10 mL) and filtered. The phases of the filtrate are separated and the aqueous phase is extracted with tert-butyl methyl ether (15 mL). The organic extracts and organic phase is combined, dried over magnesium sulfate, filtered and concentrated under vacuum. The residue is purified by chromatography (silica gel, 30 g, 33% ethyl acetate/hexane) to provide the title compound (183 mg, 42%) as a yellow oil, cis/trans/1-2+1-4 addition, 87/9.8/3.2; 1H NMR (CDCl3) 6 5.9 (m, 1H), 5.8 (m, 1H), 4.6 (m, 1H), 4.5 (m, 1H), 2.7 (m, 1H), 2.0 (d,1H, J=9.6 Hz), 1.5 (d appt, 1H, J=4.5, 14 Hz), 1.2 (s, 9H); 13C NMR (CDCl3) δ136.6, 36, 75.5, 74.4, 74, 44.6, 28.7; νmax 3395, 2974, 2938, 907, 2878, 1389, 1364, 1117, 1169, 1022 cm-1 ; MS (CI) m/e (% relative intensity) 157 (M+H+ -H2O), 57, 83 (100).