Sodium Hydroxide → HCID 57445148, Verbindung

HRID 1893632

Reaktionsgleichung

Reaktionsgleichung von HRID 1893632
[CH2:1]([O:3][C:4]1[N+:5]([O-])=[CH:6][C:7]2[C:12]([CH:13]=1)=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH3:2].[OH-].[Na+].O=P(Cl)(Cl)[Cl:19]>C(Cl)(Cl)Cl>[Cl:19][C:6]1[C:7]2[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH:13]=[C:4]([O:3][CH2:1][CH3:2])[N:5]=1

Komponenten

5

Edukt 3

HCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 686175523-ethoxyisoquinoline N-oxide

Produkt 1

HCID 57445148HCID 57445148, VerbindungAusbeute 40 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6212ChloroformLösungsmittel

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

3-Ethoxyisoquinoline N-oxide (1.15 g, 6.1 mmol) was taken up in POCl3 (5 mL) at rt and then heated to 120° C. under an atmosphere of Ar for 2 h. Following cooling to rt, the reaction was diluted with CHCl3 and poured into icewater (20 mL) and the resulting solution was placed in an ice bath and treated with 10M NaOH until pH 10 with vigorous stirring. Following extraction with CHCl3, the combined organics were washed with brine and dried over anhydrous MgSO4. Following concentration in vacuo, purification on SiO2 (3-15% EtOAc/hex) afforded 0.51 g (40%) of 1-chloro-3-ethoxyisoquinoline. LCMS found 208.1 [M+H]+.

Aufarbeitung

  1. temperatureFollowing cooling to rt
  2. additionpoured into icewater (20 mL)
  3. customthe resulting solution was placed in an ice bath
  4. extractionextraction with CHCl3
  5. washthe combined organics were washed with brine
  6. dry with materialdried over anhydrous MgSO4
  7. concentrationconcentration
  8. customin vacuo, purification on SiO2 (3-15% EtOAc/hex)

Quellen und Nachweise

ORD-Eintrag
ord-ed83c68ee98e4c88ba333c80fa3a1058
Quelldatensatz
uspto-grants-2013_08
Patentnummer
US08513186B2

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