Reacción #1018586

Ecuación de reacción

4-vinyl-1-cyclohexene 1,2-epoxide

succinic anhydride

hydroquinone

acrylic acid

TEMPO

→

4-((2-(acryloyloxy)-4-ethylcyclohexyl)oxy)-4-oxobutanoic acid

Disolventes

triethylamine

Toluene

dichloromethane

xylene

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroA round-bottom flask equipped with a stirring bar, a reflux condenser and a dropping funnel
2. 2
   Temperaturathe reaction mixture was further heated to 90° C
3. 3
   OtroAfter completion of reaction
4. 4
   Temperaturathe reaction mixture was cooled down to 70-75° C.
5. 5
   Temperaturathe reaction mixture was further heated to 90-95° C
6. 6
   OtroAfter completion of reaction
7. 7
   Temperaturathe reaction mixture was cooled down again to 75° C.
8. 8
   Lavadowashed with hot brine solution
9. 9
   Otroto remove traces of triethylamine
10. 10
    FiltraciónThe organic layer was filtered over Celite column
11. 11
    Otroto remove charcoal
12. 12
    Otroto remove traces of acrylic acid
13. 13
    FiltraciónThe organic phase was further filtered
14. 14
    Concentraciónconcentrated
15. 15
    Otroto yield pale yellow color viscous product

Procedimiento

A round-bottom flask equipped with a stirring bar, a reflux condenser and a dropping funnel was charged with 1.6 g of 4-vinyl-1-cyclohexene 1,2-epoxide, and was heated to 70-75° C. At this point catalytic amount of platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex solution in xylene, (Pt around 2%) was added and the reaction mixture was further heated to 90° C. To this reaction mixture, 10 g of monohydride functionalized polydimethylsiloxane, was added drop-wise. After completion of reaction, the reaction mixture was cooled down to 70-75° C. and 20 mL of Toluene, and a catalytic amount of Titanium isopropoxide and TEMPO (2,2,6,6-Tetramethylpiperidine 1-oxyl) was added and the reaction mixture was further heated to 90-95° C. To this reaction mixture, 1.7 g of acrylic acid, was added drop-wise over a period of two hours. The reaction was monitored using 1H-NMR spectroscopy. After completion of reaction, the reaction mixture was cooled down again to 75° C. and 2.5 g of succinic anhydride, 2.5 g of triethylamine, and 300 ppm of hydroquinone was added. The reaction was monitored using 1H-NMR spectroscopy. After completion the product was vacuum striped, re-dissolved in dichloromethane and washed with hot brine solution. The organic phase was passed over Tulsion T66-MP resin to remove traces of triethylamine and decolorized using activated charcoal. The organic layer was filtered over Celite column to remove charcoal and then stirred along with Dowex WBA resin to remove traces of acrylic acid. The organic phase was further filtered and concentrated to yield pale yellow color viscous product.

Fuente