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Lithium Carbonate → 9-Benzyl-6-methoxy-9H-carbazol-4-ol

HRID 1057655
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1057655
[CH2:1]([N:8]1[C:20]2[CH2:19][CH2:18][CH2:17][C:16](=[O:21])[C:15]=2[C:14]2[C:9]1=[CH:10][CH:11]=[C:12]([O:22][CH3:23])[CH:13]=2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O1CCOCC1.[Br-].[Li+].C(=O)([O-])[O-].[Li+].[Li+]>C(O)CO.[Cu](Cl)Cl>[CH2:1]([N:8]1[C:20]2[CH:19]=[CH:18][CH:17]=[C:16]([OH:21])[C:15]=2[C:14]2[C:9]1=[CH:10][CH:11]=[C:12]([O:22][CH3:23])[CH:13]=2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 11125Lithium CarbonateHCID 312751,4-DioxaneHCID 82050Lithium BromideHCID 111095159-Benzyl-6-methoxy-1,2,3,9-tetrahydro-4H-carbazol-4-one

Produkt 1

HCID 97964539-Benzyl-6-methoxy-9H-carbazol-4-olAusbeute 73 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 24014
Cupric Chloride
Katalysator
HCID 174Ethylene GlycolLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a mixture of 9-benzyl-6-methoxy-1,2,3,9-tetrahydro-4H-carbazol-4-one (4.23 g, 13.85 mmol) in ethylene glycol: p-dioxane ((1:1) 150 mL) is added copper (II) chloride (9.31 g, 69.26 mmol). The mixture is heated at 80° C. for 30 minutes. The mixture is partitioned between water and Et2O. The layers are separated and the organic layer washed with water (100 mL). The ether layer is dried over anhydrous sodium sulfate, filtered and concentrated. The residue is dissolved in DMF (50 mL) to which is added lithium bromide (2.45 g, 28.3 mmol) and lithium carbonate (2.09 g, 28.3 mnmol). The mixture is heated at 120° C. for 5 h. The mixture is partitioned between water and ethyl acetate. The layers are separated and the organic layer washed twice with water (200 mL). Column chromatography (250 mL) silica gel using ethyl acetate/ hexanes (20/80) gave 2.5 g (73%) of the title compound; IR (drift) 3471, 1482, 1469, 1450, 1328, 1198, 1171, 1144, 805, 799, 780, 745, 724, 717, 701 cm−1. 1H NMR (DMSO-d6) δ3.82, 5.54, 6.56, 6.97), 7.14, 7.23, 7.43, 7.72; Anal. Calcd for C20H17NO2: C, 79.18; H, 5.65; N, 4.62. Found: C, 78.99; H, 5.75; N, 4.63.

Aufarbeitung

  1. customThe mixture is partitioned between water and Et2O
  2. customThe layers are separated
  3. washthe organic layer washed with water (100 mL)
  4. dry with materialThe ether layer is dried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. dissolutionThe residue is dissolved in DMF (50 mL) to which
  8. temperatureThe mixture is heated at 120° C. for 5 h
  9. customThe mixture is partitioned between water and ethyl acetate
  10. customThe layers are separated
  11. washthe organic layer washed twice with water (200 mL)

Quellen und Nachweise

ORD-Eintrag
ord-ac4d131f7c31461d881ca44338bdbbf2
Quelldatensatz
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06514968B1

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