Reaktion #7786

ord-e5f24134709a4e5289eb9e087aef7de8

Reaktionsgleichung

Cc1ccc(-c2nc3ccccc3o2)cc1-c1cccc(C#N)c1
5′-(1,3-benzoxazol-2-yl)-2′-methyl-1,1′-biphenyl-3-carbonitrile
O=C1CCC(=O)N1Br
n-bromosuccinimide
O=C(OOC(=O)c1ccccc1)c1ccccc1
benzoyl peroxide
N#Cc1cccc(-c2cc(-c3nc4ccccc4o3)ccc2CBr)c1
5′-(1,3-benzoxazol-2-yl)-2′-(bromomethyl)-1,1′-biphenyl-3-carbonitrile

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas refluxed for 5 h
  2. 2
    SonstigeThe solvent was evaporated to dryness
  3. 3
    Sonstigethe crude was purified by flash chromatography on silica gel eluting with a gradient of EtOAc

Vorschrift

A mixture of 5′-(1,3-benzoxazol-2-yl)-2′-methyl-1,1′-biphenyl-3-carbonitrile (229 mg, 0.74 mmol), n-bromosuccinimide (145 mg, 0.81 mmol), and benzoyl peroxide (9 mg, 0.037 mmol) in carbon tetrachloride (15 mL) was refluxed for 5 h. The solvent was evaporated to dryness and the crude was purified by flash chromatography on silica gel eluting with a gradient of EtOAc:hexanes (0 to 30 min: 0 to 20% EtOAc, 30 to 40 min: 50% EtOAc) to afford 5′-(1,3-benzoxazol-2-yl)-2′-(bromomethyl)-1,1′-biphenyl-3-carbonitrile as a colorless solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087601B2uspto-grants-2006_08