Hydrochloric Acid → 6-Fluoro-2-methyl-2,3-dihydroquinolin-4(1H)-one

HRID 1287621Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1287621
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][CH:6]=[C:5]2[O:12]C.[CH3:14][Li].Cl>O1CCCC1.C(OCC)C>[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH:7]([CH3:14])[CH2:6][C:5]2=[O:12]

Komponenten

6

Reaktionsbedingungen

Temperatur
-20 °C

Versuchsvorschrift

A stirred solution of 25.8 g (0.146 mole) of 6-fluoro-4-methoxyquinoline from example 3 in 300 ml of tetrahydrofuran was heated under a nitrogen atmosphere to its reflux temperature and then cooled to -20° C. To the cold solution was added 90 ml of 182 M methyl lithium in diethyl ether over a period of 0.5 hour. After adding 40 ml of the solution, the reaction temperature was allowed to rise to 0° C. After the addition of methyl lithium was completed, the reaction temperature was allowed to rise to 15° C. The solution was then poured into 1200 ml of a mixture of ice water and hydrochloric acid. After stirring for 0.5 hour the mixture was extracted with about 1200 ml of diethyl ether. The organic layer was dried, filtered and evaporated in vacuo to provide a yellow solid. The product was recrystallized from carbon tetrachloride to give 9.5 g. (37% yield) of 6-fluoro-2-methyl-4-oxo-1,2,3,4-tetrahydroquinoline.

Aufarbeitung

  1. temperaturereflux temperature
  2. customto rise to 0° C
  3. customto rise to 15° C
  4. extractionwas extracted with about 1200 ml of diethyl ether
  5. customThe organic layer was dried
  6. filtrationfiltered
  7. customevaporated in vacuo
  8. customto provide a yellow solid
  9. customThe product was recrystallized from carbon tetrachloride
  10. customto give 9.5 g

Quellen und Nachweise

ORD-Eintrag
ord-73cbcd27466a4d74a49e83ceb3821f48
Quelldatensatz
uspto-grants-1976_10
Patentnummer
US03985753

Notizen zur Reaktion

Wird geladen…