Reacción #1148665

ord-830ae300d2794a8aa4c9d3e0dc32c6e1

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas removed in vacuo
  2. 2
    TemperaturaThe solids were cooled to −78° C.
  3. 3
    TemperaturaThe solution was warmed to room temperature
  4. 4
    workup.WAITkept there overnight
  5. 5
    FiltraciónThe resulting yellow-orange turbid solution was then filtered over a plug of Celite
  6. 6
    Lavadothe Celite was washed with CH2Cl2 until the washings
  7. 7
    OtroThe product was recrystallized from CH2Cl2/hexane at −18° C
  8. 8
    OtroC, H analysis (crystallizes with CH2Cl2)

Procedimiento

N-Butyllithium (1.6 M in hexanes, 4.2 mL, 6.7 mmol) was added dropwise to a solution of 2-(4-methyl)phenyl)indene (1.323 g, 6.4 mmol) in Et2O (20 mL). The red-orange solution was stirred at ambient temperature for 30 min after which time the solvent was removed in vacuo. In a drybox, to the resulting solid was added ZrCl4 (0.754 g, 3.2 mmol). The solids were cooled to −78° C. and methylene chloride (60 mL) was slowly added. The solution was warmed to room temperature and kept there overnight. The resulting yellow-orange turbid solution was then filtered over a plug of Celite and the Celite was washed with CH2Cl2 until the washings were colorless (ca. 60 mL). The product was recrystallized from CH2Cl2/hexane at −18° C. Yield: 577 mg (31%). 1H NMR (C6D6, 23° C., 400 MHz): δ 7.36 (d, J=8 Hz, 4H); 7.11 (m, 4H); 7.02 (d, J=8 Hz, 4H); 6.92 (m, 4H); 6.43 (s, 4H, Cp-H); 2.17 (s, 6H, CH3). C, H analysis (crystallizes with CH2Cl2): Anal. Found (Calcd.): C, 63.21 (63.46); H, 4.41 (4.42).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06960550B2uspto-grants-2005_11