Reaktion #955948

ord-089e894bbbd949f7a193802e14b14d78

Reaktionsgleichung

Cc1cc2ccccc2c2ccccc12
9-methylphenanthrene
O=C1CCC(=O)N1Br
NBS
BrCc1cc2ccccc2c2ccccc12
product
Ausbeute 89.7%
BrCc1cc2ccccc2c2ccccc12
9-(bromomethyl)phenanthrene
Ausbeute 89.7%

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas refluxed for 5 h
  2. 2
    Sonstigethe succinimide precipitated
  3. 3
    Sonstigewas removed by filtration
  4. 4
    WaschenThe filtrate was washed by 15% NaOH
  5. 5
    Trocknendried over MgSO4
  6. 6
    Einengenconcentrated

Vorschrift

A mixture of 9-methylphenanthrene (14.2 g, 74 mmol), benzoyl peroxide (40 mg, 0.16 mmol) and NBS (13.3 g, 74.6 mmol) in 210 mL of benzene was refluxed for 5 h. The reaction mixture was cooled to 0° C. and the succinimide precipitated was removed by filtration. The filtrate was washed by 15% NaOH, dried over MgSO4 and concentrated to yield 18 g of product which was used for the next step without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08968887B2uspto-grants-2015_03