Potassium Hydroxide → 1-Hydroxy-1-(perfluoroethyl)-2,3,4,9-tetrahydro-1H-carbazole-6-carbonitrile

HRID 877462Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 877462
[F:1][C:2]([F:37])([C:7]1([O:32][Si](C)(C)C)[C:19]2[N:18](S(C3C=CC(C)=CC=3)(=O)=O)[C:17]3[C:12](=[CH:13][C:14]([C:30]#[N:31])=[CH:15][CH:16]=3)[C:11]=2[CH2:10][CH2:9][CH2:8]1)[C:3]([F:6])([F:5])[F:4].[OH-].[K+]>C1COCC1.O>[OH:32][C:7]1([C:2]([F:37])([F:1])[C:3]([F:4])([F:5])[F:6])[C:19]2[NH:18][C:17]3[C:12](=[CH:13][C:14]([C:30]#[N:31])=[CH:15][CH:16]=3)[C:11]=2[CH2:10][CH2:9][CH2:8]1

Komponenten

5

Versuchsvorschrift

To a solution of 1-(perfluoroethyl)-9-tosyl-1-(trimethylsilyloxy)-2,3,4,9-tetrahydro-1H-carbazole-6-carbonitrile (180 mg, 0.3 mmol) in THF (5 mL), KOH (90 mg, 1.6 mmol) in H2O (1 mL) was added. The reaction mixture was refluxed for 20 h, diluted with water and extracted with EtOAc (3×20 mL). The combined organic extracts were dried over Na2SO4 and concentrated under reduced pressure to give the crude residue which was purified by column chromatography [EtOAc-hexane (1:19) as eluant] to afford the title compound as a white solid (40 mg, 40%). 1H NMR (500 MHz, CDCl3, δ in ppm) 8.5 (bs, 1H), 7.9 (s, 1H), 7.49 (d, J=7.5 Hz, 1H), 7.44 (d, J=7.5 Hz, 1H), 2.90-2.86 (m, 1H), 2.74-2.56 (m, 1H), 2.56 (s, 1H), 2.33-2.29 (m, 1H), 2.20-2.12 (m, 2H), 2.04-2.03 (m, 1H).

Aufarbeitung

  1. temperatureThe reaction mixture was refluxed for 20 h
  2. extractionextracted with EtOAc (3×20 mL)
  3. dry with materialThe combined organic extracts were dried over Na2SO4
  4. concentrationconcentrated under reduced pressure
  5. customto give the crude residue which
  6. customwas purified by column chromatography [EtOAc-hexane (1:19) as eluant]

Quellen und Nachweise

ORD-Eintrag
ord-df864dabd347437f95b14a08aff6b950
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08987319B2

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