Réaction #216128

ord-57fb6aee93a8490fa259b1e7effc360c

Équation de réaction

Brc1cnc2ccccc2c1
3-bromoquinoline
C#CCCO
3-butyn-1-ol
OCCC#Cc1cnc2ccccc2c1
oil
Rendement 136.9%
OCCC#Cc1cnc2ccccc2c1
4-(3-Quinolinyl)-3-butyn-1-ol
Rendement 136.9%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreby bubbling in dry nitrogen for 15 minutes
  2. 2
    AutreThe flask is flushed with nitrogen
  3. 3
    Températurethe mixture is heated
  4. 4
    Températureto reflux for 5 hours
  5. 5
    workup.ADDITIONThe cooled mixture is diluted with dichloromethane
  6. 6
    Lavagewashed with water
  7. 7
    Séchagedried (sodium sulfate)
  8. 8
    Concentrationconcentrated

Mode opératoire

A solution of 3-bromoquinoline (13.57 mL, 0.10 mol) and 3-butyn-1-ol (9.0 mL, 0.12 mol) in 40 mL of triethylamine and 75 mL of dichloromethane is degassed by bubbling in dry nitrogen for 15 minutes, and 0.7 g (0.001 mol) of bis(triphenylphosphine)palladium chloride and 0.013 g of cuprous iodide are added. The flask is flushed with nitrogen and the mixture is heated to reflux for 5 hours. The cooled mixture is diluted with dichloromethane and washed with water, dried (sodium sulfate), and concentrated to give 27 g of an oil. The oil is triturated with diethyl ether to give 18.2 g of the title compound as a tan solid; mp 95.7°-96.7° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05466698uspto-grants-1995_11