Реакция #2358495
ord-10add070db8b47538972f12ce1d018fc
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1Температураthe reaction mixture was warmed up to −40° C.
- 2workup.STIRRINGstirred for 5 min
- 3ТемператураThe mixture was warmed up to 0° C.
- 4workup.STIRRINGstirred for another 30 min
- 5ТемператураThe reaction mixture was warmed up to room temperature
- 6workup.STIRRINGstirred for 3 h
- 7Другоеthe layers were separated
- 8ЭкстракцияThe aqueous layer was extracted with ethyl acetate
- 9Промывкаwashed with water and brine
- 10Сушкаdried over Na2SO4
- 11Другоеthe solvent was evaporated
- 12Другоеto give a brown residue which
- 13Другоеwas purified by flash chromatography (0-100% ethyl acetate in cyclohexane)
Методика
1-Phenylazepan-2-one (0.500 g, as prepared in Organic Letters 2000, pages 1101-1104) was dissolved in tetrahydrofuran (30 mL) and cooled to −78° C. To the solution was added LDA (2.0 mol/L in THF/heptane/ethylbenzene, 2.6 mL) dropwise. After stirring for 10 min between −55 and −50° C., the reaction mixture was warmed up to −40° C., stirred for 5 min and ethylformate (0.657 mL, 0.605 g) was added slowly. The mixture was warmed up to 0° C. and stirred for another 30 min. 2-Chloro-4-methyl-2H-furan-5-one (0.420 g in 2 mL of THF) was added dropwise. The reaction mixture was warmed up to room temperature and stirred for 3 h. Water and ethyl acetate were added and the layers were separated. The aqueous layer was extracted with ethyl acetate, the organic layers were combined, washed with water and brine, dried over Na2SO4 and the solvent was evaporated to give a brown residue which was purified by flash chromatography (0-100% ethyl acetate in cyclohexane). (3E)-3-[(4-methyl-5-oxo-2H-furan-2-yl)oxymethylene]-1-phenyl-azepan-2-one Ic-13 (0.103 g, 11%) was obtained as a white solid; mp: 150-160° C.; LCMS (Method D): 0.91 min; ES+314 (M+H+).