Isopropanol → 4-[(E)-2-cyclohexylethenyl]-2-fluoroaniline

HRID 576079Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 576079
C(O)(C)C.C(O[K])(C)(C)C.[CH:11]1(/[CH:17]=[CH:18]/B(O)O)[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1.Br[C:23]1[CH:29]=[CH:28][C:26]([NH2:27])=[C:25]([F:30])[CH:24]=1>ICCC.O>[CH:11]1(/[CH:17]=[CH:18]/[C:23]2[CH:29]=[CH:28][C:26]([NH2:27])=[C:25]([F:30])[CH:24]=2)[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1

Komponenten

7

Versuchsvorschrift

Isopropanol (60 mL) was added to PEPPSI™-IPr catalyst (161 mg, 0.24 mmol) and tert-butoxy potassium (2.65 g, 23.6 mmol) under an argon atmosphere, and the mixture was stirred at room temperature for 15 min. To the reaction mixture were added trans-(2-cyclohexylvinyl)boronic acid (2.00 g, 13.0 mmol) and 4-bromo-2-fluoroaniline (2.24 g, 11.8 mmol) successively and the mixture was stirred at room temperature for 15 hr. Water was added thereto, the mixture was extracted with ethyl acetate, and the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure to afford 4-[(E)-2-cyclohexylethenyl]-2-fluoroaniline as a reddish brown oil (2.58 g).

Aufarbeitung

  1. stirringthe mixture was stirred at room temperature for 15 hr
  2. extractionthe mixture was extracted with ethyl acetate
  3. washthe organic layer was washed with brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationThe desiccant was filtered off
  6. concentrationthe filtrate was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-c09a1b39f8f547cabadb0c5a76a78547
Quelldatensatz
uspto-grants-2015_05
Patentnummer
US09035059B2

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