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Ethylene → Ethylene Vinylethylene Carbonate

HRID 2288943
ノート
印刷プレビュー

反応式

HRID 2288943 の反応式
C=C.[C:3](=[O:6])([OH:5])[OH:4].[CH:7]([CH:9]=[CH2:10])=[CH2:8]>>[CH2:7]=[CH2:8].[C:3]1(=[O:5])[O:4][CH2:10][CH:9]([CH:7]=[CH2:8])[O:6]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 6325EthyleneHCID 56924127Buta-1,3-diene;carbonic acid

生成物 1

HCID 86755542Ethylene Vinylethylene Carbonate

反応条件

温度
23 °C

実験手順

A 200 mL flame dried pear-shaped Schlenk flask equipped with a magnetic stir bar and capped with a septum was charged with (2,6-di-isopropylphenylimino)-1,4-dithiane Pd(II) catalyst XII (100 mg) in an argon filled glove box. Upon removal from the glove box, the flask was evacuated and backfilled with ethylene. The catalyst was dissolved in CH2Cl2 (20 mL) and immediately treated with vinyl ethylene carbonate (10 mL). The resulting orange solution was stirred at 23° C. under an ethylene atmosphere (1 atm) for 28 hours. A small amount of polymer had precipitated out of solution. The polymerization was quenched with MeOH and acetone leaving gray oil adhering to the walls of the flask. The polymer was dissolved in CH2Cl2 and transferred to a storage jar. The solvent was left to evaporate and the resulting oily polymer. The polymer was washed several times with acetone and MeOH to remove any remaining monomer and was dried in vacuo at ~80° C. for 1 day to afford a tacky solid (1.15 g, 613 TO). 1H NMR was consistent with a copolymer containing approximately 95.5 weight % ethylene and 4.5 weight % vinyl ethylene carbonate monomer units.; Mn 15,400 g /mol ; Mw 96,000 g /mol ; DSC Tg -64° C., Tm -31° C.

後処理

  1. temperatureA 200 mL flame dried pear-shaped Schlenk flask
  2. customequipped with a magnetic stir bar
  3. customcapped with a septum
  4. customUpon removal from the glove box
  5. customthe flask was evacuated
  6. dissolutionThe catalyst was dissolved in CH2Cl2 (20 mL)
  7. additionimmediately treated with vinyl ethylene carbonate (10 mL)
  8. customA small amount of polymer had precipitated out of solution
  9. customThe polymerization was quenched with MeOH and acetone leaving gray oil adhering to the walls of the flask
  10. dissolutionThe polymer was dissolved in CH2Cl2
  11. waitThe solvent was left
  12. customto evaporate
  13. washThe polymer was washed several times with acetone and MeOH
  14. customto remove any remaining monomer
  15. customwas dried in vacuo at ~80° C. for 1 day
  16. customto afford a tacky solid (1.15 g, 613 TO)
  17. customDSC Tg -64° C., Tm -31° C.

出典と根拠

ORDレコード
ord-3f779558e3264fc6a0e1764f984fb97b
出典データセット
uspto-grants-2000_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06090900

反応ノート

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