Sodium Hydroxide → 6-Chloro-3-methylisoquinoline

HRID 1968731

Reaktionsgleichung

Reaktionsgleichung von HRID 1968731
[Cl:1][C:2]1[CH:16]=[CH:15][C:5]([CH2:6]/[N:7]=[C:8](/[CH3:14])\[CH:9](OC)OC)=[CH:4][CH:3]=1.[OH-].[Na+]>>[Cl:1][C:2]1[CH:16]=[C:15]2[C:5](=[CH:4][CH:3]=1)[CH:6]=[N:7][C:8]([CH3:14])=[CH:9]2

Komponenten

3

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

During 10 min. (4-chloro-benzyl)-[2,2-dimethoxy-1-methyl-eth-(Z)-ylidene]-amine (120 g, 0.496 mol) was added dropwise to polyphosphoric acid (1000 g) at 130° C. The resulting reaction mixture was heated for 3 h at 140° C. After cooling below 100° C. the reaction mixture was poured onto ice (1 kg) and neutralized (pH=7) with a 33% aqueous NaOH solution. Care was taken that the temperature did not rise above 35° C. by adding additional ice. The reaction mixture was extracted with dichloromethane (3×1 L) and the combined organic layers were dried over Na2SO4, filtered and concentrated at reduced pressure to afford a black oil. The crude product was purified bulb-to-bulb distillation (105-110° C., 2 mbar) to afford the title compound as colorless oil which crystallized upon standing (66.7 g, 0.375 mol, 76%). MS (ES+): 178 (M(C10H835ClN)+H)+.

Aufarbeitung

  1. customThe resulting reaction mixture
  2. temperatureAfter cooling below 100° C. the reaction mixture
  3. customdid not rise above 35° C.
  4. additionby adding additional ice
  5. extractionThe reaction mixture was extracted with dichloromethane (3×1 L)
  6. dry with materialthe combined organic layers were dried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated at reduced pressure
  9. customto afford a black oil
  10. customThe crude product was purified
  11. distillationbulb-to-bulb distillation (105-110° C., 2 mbar)

Quellen und Nachweise

ORD-Eintrag
ord-c764924bfb3248c4ad60a91f30363388
Quelldatensatz
uspto-grants-2013_04
Patentnummer
US08426440B2

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