Reaktion #52640

ord-755aa668e775454ba249d41e3461328d

Reaktionsgleichung

Clc1ccc(OCCN2CCOCC2)c(C2CCCCC2)c1
3-cyclohexyl-4-morpholinoethoxychlorobenzene
c1ccc2ccccc2c1
Naphthalene
[Li]
lithium
CN(C)C=O
Dimethylformamide
O=Cc1ccc(OCCN2CCOCC2)c(C2CCCCC2)c1
3-cyclohexyl-4-morpholinoethoxybenzaldehyde
Ausbeute 38.3%

Reaktionsbedingungen

Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstige(approximately 1 hour)
  2. 2
    Temperaturthe reaction was warmed to 0° C.
  3. 3
    workup.STIRRINGstirred for an additional hour
  4. 4
    workup.STIRRINGthe reaction was stirred at 0° C. for one more hour
  5. 5
    Temperaturwarmed to room temperature
  6. 6
    workup.STIRRINGstirred for another hour
  7. 7
    SonstigeThe reaction was quenched with methanol (30 ml)
  8. 8
    workup.ADDITIONadded to 1N hydrochloric acid (300 ml)
  9. 9
    Extraktionextracted with ethyl acetate (400 ml)
  10. 10
    WaschenThe organic layer was washed with water (300 ml), saturated sodium bicarbonate solution (300 ml) and brine (300 ml)
  11. 11
    Trocknendried over magnesium sulfate
  12. 12
    Einengenconcentrated

Vorschrift

Naphthalene (3.48 g, 27.2 mmol) was added to a suspension of 30% lithium dispersion (3.2 g, 138 mmol, pre-washed with tetrahydrofuran) in tetrahydrofuran (80 ml). The suspension was stirred until a green color appeared (approximately 1 hour). The reaction was cooled to −78° C., and a solution of the 3-cyclohexyl-4-morpholinoethoxychlorobenzene (8 g, 24.7 mmol) in tetrahydrofuran (20 ml) was added. After 1 hour, the reaction was warmed to 0° C. and stirred for an additional hour. Dimethylformamide (9.6 ml, 123.5 mmol) was added, the reaction was stirred at 0° C. for one more hour and then warmed to room temperature and stirred for another hour. The reaction was quenched with methanol (30 ml), added to 1N hydrochloric acid (300 ml) and extracted with ethyl acetate (400 ml). The organic layer was washed with water (300 ml), saturated sodium bicarbonate solution (300 ml) and brine (300 ml), dried over magnesium sulfate and concentrated. Chromatography (silica, 40-60% ethyl acetate/hexanes) afforded 3 g (34%) of 3-cyclohexyl-4-morpholinoethoxybenzaldehyde as a light yellow oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06855730B2uspto-grants-2005_02