Реакция #2358495

ord-10add070db8b47538972f12ce1d018fc

Уравнение реакции

CC1=CC(Cl)OC1=O
2-Chloro-4-methyl-2H-furan-5-one
CC(C)[N-]C(C)C.[Li+]
LDA
O=C1CCCCCN1c1ccccc1
1-Phenylazepan-2-one
CCOC=O
ethylformate
CC1=CC(O/C=C2\CCCCN(c3ccccc3)C2=O)OC1=O
(3E)-3-[(4-methyl-5-oxo-2H-furan-2-yl)oxymethylene]-1-phenyl-azepan-2-one

Растворители

Условия реакции

Температура
-78°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe reaction mixture was warmed up to −40° C.
  2. 2
    workup.STIRRINGstirred for 5 min
  3. 3
    ТемператураThe mixture was warmed up to 0° C.
  4. 4
    workup.STIRRINGstirred for another 30 min
  5. 5
    ТемператураThe reaction mixture was warmed up to room temperature
  6. 6
    workup.STIRRINGstirred for 3 h
  7. 7
    Другоеthe layers were separated
  8. 8
    ЭкстракцияThe aqueous layer was extracted with ethyl acetate
  9. 9
    Промывкаwashed with water and brine
  10. 10
    Сушкаdried over Na2SO4
  11. 11
    Другоеthe solvent was evaporated
  12. 12
    Другоеto give a brown residue which
  13. 13
    Другоеwas 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+).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09119398B2uspto-grants-2015_09