反応 #1018586

反応方程式

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

succinic anhydride

hydroquinone

acrylic acid

TEMPO

→

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

溶媒

triethylamine

Toluene

dichloromethane

xylene

反応条件

後処理

1. 1
   その他A round-bottom flask equipped with a stirring bar, a reflux condenser and a dropping funnel
2. 2
   温度the reaction mixture was further heated to 90° C
3. 3
   その他After completion of reaction
4. 4
   温度the reaction mixture was cooled down to 70-75° C.
5. 5
   温度the reaction mixture was further heated to 90-95° C
6. 6
   その他After completion of reaction
7. 7
   温度the reaction mixture was cooled down again to 75° C.
8. 8
   洗浄washed with hot brine solution
9. 9
   その他to remove traces of triethylamine
10. 10
    ろ過The organic layer was filtered over Celite column
11. 11
    その他to remove charcoal
12. 12
    その他to remove traces of acrylic acid
13. 13
    ろ過The organic phase was further filtered
14. 14
    濃縮concentrated
15. 15
    その他to yield pale yellow color viscous product

実験手順

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.

出典