Réaction #7432

Équation de réaction

2-Chloro-isoquinoline

phenylboronic acid

triphenylphosphine

potassium carbonate

→

1-phenylisoquinoline

Rendement 96.9%

Solvants

dimethoxyethane

Conditions de réaction

Traitement

1. 1
   Températureat reflux for 17 hrs
2. 2
   TempératureThe mixture was then cooled
3. 3
   Autrethe aqueous layer was separated from the organic layer
4. 4
   ExtractionThe aqueous extraction
5. 5
   Extractionwas then extracted with ethyl acetate
6. 6
   ExtractionThe combined organic extractions
7. 7
   Extractionwere then extracted with brine
8. 8
   Séchagedried over magnesium sulfate
9. 9
   AutreThe solvent was then evaporated
10. 10
    Autreto give a liquid which
11. 11
    workup.DISTILLATIONwas then purified by Kugelhor distillation at 220° C. @1200 microns

Mode opératoire

2-Chloro-isoquinoline (28.8 g, 0.176 mol), phenylboronic acid (25.7 g 0.211 mol), triphenylphosphine (4.6 g 17.6 mmol), palladium acetate (0.99 g 4.4 mmol) and 2M solution of potassium carbonate (65.7 g 0.475 mol) were added to 270 ml of dimethoxyethane. This mixture was stirred at reflux for 17 hrs. The mixture was then cooled and the aqueous layer was separated from the organic layer. The aqueous extraction was then extracted with ethyl acetate. The combined organic extractions were then extracted with brine and dried over magnesium sulfate. The solvent was then evaporated to give a liquid which was then purified by Kugelhor distillation at 220° C. @1200 microns to yield 35 g (96.9%) of 1-phenylisoquinoline.

Source