Reaktion #68720

Reaktionsgleichung

1,4-Diiodobenzene

Triethylamine

formic acid

4,4′-(bicyclo[2.2.1]hept-5-en-2-ylmethylene)bis(2-methylphenol)

ethyl acetate

→

4,4′-((5-(4-(5-(bis(4-hydroxy-3-methylphenyl)methyl)bicyclo[2.2.1]heptan-2-yl)phenyl) bicyclo[2.2.1]heptan-2-yl)methylene)bis(2-methylphenol)

Ausbeute 60.0%

Lösungsmittel

DMF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONcharged to an appropriately sized reaction vessel
2. 2
   Sonstigeequipped
3. 3
   Sonstigea reflux condenser and placed under a nitrogen atmosphere
4. 4
   workup.STIRRINGwith stirring to this mixture
5. 5
   TemperaturDuring the course of heating the mixture
6. 6
   SonstigeThe temperature of the reaction mixture rose to 119° C. due to the exotherm of the reaction
7. 7
   workup.STIRRINGto stir overnight (16 hours) at 75° C. in the oil bath
8. 8
   SonstigeThe reaction mixture obtained
9. 9
   Filtrationfiltered through a silica gel plug
10. 10
    WaschenThe filtrate was washed with water
11. 11
    Sonstigethe organic layer obtained
12. 12
    Trocknenwas dried over anhydrous MgSO4
13. 13
    SonstigeThe crude mixture was purified with medium pressure column chromatography
14. 14
    SonstigeThis separation
15. 15
    Sonstigeresulted in the isolation of 9.5 g of the PP719 (60% yield; 95% purity)

Vorschrift

1,4-Diiodobenzene (7.51 g; 22.8 mmol), (tris-o-tolylphosphine)2PdCl2 (0.713 g, 0.907 mmol), 4,4′-(bicyclo[2.2.1]hept-5-en-2-ylmethylene)bis(2-methylphenol) (21.8 g; 68.0 mmol) and DMF (100 mL) were weighed and charged to an appropriately sized reaction vessel equipped with stirring and a reflux condenser and placed under a nitrogen atmosphere. Triethylamine (19.0 mL, 136 mmol) and formic acid (4.40 mL, 117 mmol) were then added with stirring to this mixture. The mixture was heated to 75° C. using an oil bath. During the course of heating the mixture changed from yellow to orange and became clear. The temperature of the reaction mixture rose to 119° C. due to the exotherm of the reaction and the solution became darker, with gas evolution. The reaction mixture was allowed to stir overnight (16 hours) at 75° C. in the oil bath. The reaction mixture obtained was a clear yellow solution with black palladium particles present. The reaction mixture was diluted with ethyl acetate (100 ml) and filtered through a silica gel plug. The filtrate was washed with water and the organic layer obtained was dried over anhydrous MgSO4. The crude mixture was purified with medium pressure column chromatography and the eluting solution was gradually changed from 100% hexanes to 100% ethyl acetate. This separation resulted in the isolation of 9.5 g of the PP719 (60% yield; 95% purity). The identity of the product was confirmed by as PP719 by LC-MS (ES1) and proton NMR.

Quelle