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Acetic Anhydride → 5,6,7,8-Tetrahydroquinolin-8-yl acetate

HRID 2301140
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2301140
[N+:1]1([O-])[C:10]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[C:12]([O:15]C(=O)C)(=[O:14])[CH3:13]>>[C:12]([O:15][CH:9]1[C:10]2[N:1]=[CH:2][CH:3]=[CH:4][C:5]=2[CH2:6][CH2:7][CH2:8]1)(=[O:14])[CH3:13]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 7918Acetic AnhydrideHCID 27781345,6,7,8-Tetrahydro-1-quinoliniumolate

Produkt 1

HCID 122262495,6,7,8-Tetrahydroquinolin-8-yl acetateAusbeute 33 %

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

5,6,7,8-Tetrahydroquinoline N-oxide (1.6 g, 11 mmol) was mixed with acetic anhydride (9.2 ml) and stirred at 90° C. for 7 hours. After removing the solvent by evaporation under a reduced pressure, the residue was neutralized with sodium hydroxide aqueous solution (1 N) and the reaction product was extracted with chloroform. The extract was washed with saturated brine and dried with anhydrous sodium sulfate, and then the solvent was removed by evaporation under a reduced pressure and the thus obtained material was separated and purified by a silica gel column chromatography to obtain 690 mg (3.6 mmol, 33%) of the title compound.

Aufarbeitung

  1. customAfter removing the solvent
  2. customby evaporation under a reduced pressure
  3. extractionthe reaction product was extracted with chloroform
  4. washThe extract was washed with saturated brine
  5. dry with materialdried with anhydrous sodium sulfate
  6. customthe solvent was removed by evaporation under a reduced pressure
  7. customthe thus obtained material was separated
  8. custompurified by a silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-63fbf13115b54df1b80ed99559a6b0e5
Quelldatensatz
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06498251B1

Notizen zur Reaktion

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