Potassium acrylate → 1-Acryloyloxyethyl 4-acryloyloxybutyl carbonate

HRID 260624

反応式

HRID 260624 の反応式
[C:1](=[O:16])([O:6][CH2:7][CH2:8][CH2:9][CH2:10][O:11][C:12](=[O:15])[CH:13]=[CH2:14])[O:2][CH:3](Cl)[CH3:4].[C:17]([O-:21])(=[O:20])[CH:18]=[CH2:19].[K+]>CN(C)C=O.C1OCCOCCOCCOCCOCCOC1>[C:1](=[O:16])([O:6][CH2:7][CH2:8][CH2:9][CH2:10][O:11][C:12](=[O:15])[CH:13]=[CH2:14])[O:2][CH:3]([O:21][C:17](=[O:20])[CH:18]=[CH2:19])[CH3:4]

参加物

5

実験手順

1-Chloroethyl 4-acryloyloxybutyl carbonate (1.253 g, 5.00 mmol) prepared as described in Preparation 10 is added to a suspension of freeze dried potassium acrylate (0.606 g, 5.50 mmol) and 18-crown-6 (0.066 g, 0.25 mmol) in dimethylformamide (50 ml) under a dry N2 atmosphere. After 5 days at 20° C. the solvent is removed under reduced pressure and the residue dissolved by adding dichloromethane (60 ml) and water (30 ml). After separating the phases the aqueous layer is extracted with dichloromethane (3×30 ml) and the combined organic phase washed with saturated aqueous sodium hydrogen carbonate (50 ml). The organic phase is dried (MgSO4) and the solvent removed under reduced pressure to give 1.28 g (89%) of the title product. 1H NMR (60 MHz, CDCl3): δ 1.58 (3 H, d, J=5 Hz, CH3 --CH), 1.80 (4 H, m, CH2 --CH2), 4.24 (4 H, m, 2×CH2 --O), 5.7-6.7 (6 H, m, 2×CH=CH2), 6.87 (1 H, k, J=5 Hz, CH--CH3).

後処理

  1. customas described in Preparation 10
  2. customAfter 5 days at 20° C. the solvent is removed under reduced pressure
  3. dissolutionthe residue dissolved
  4. additionby adding dichloromethane (60 ml) and water (30 ml)
  5. customAfter separating the phases the aqueous layer
  6. extractionis extracted with dichloromethane (3×30 ml)
  7. washthe combined organic phase washed with saturated aqueous sodium hydrogen carbonate (50 ml)
  8. dry with materialThe organic phase is dried (MgSO4)
  9. customthe solvent removed under reduced pressure

出典と根拠

ORDレコード
ord-99da5765368d4b06ab6b4726afc49c5b
出典データセット
uspto-grants-1996_06
特許番号
US05529766

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