Ethylene glycol monoallyl ether → Methyl (2-allyloxy-ethoxy)-acetate

HRID 1522925

반응식

HRID 1522925 반응식
[CH2:1]([O:4][CH2:5][CH2:6][OH:7])[CH:2]=[CH2:3].[H-].[Na+].Br[CH2:11][C:12]([O:14][CH3:15])=[O:13]>C1COCC1>[CH3:15][O:14][C:12](=[O:13])[CH2:11][O:7][CH2:6][CH2:5][O:4][CH2:1][CH:2]=[CH2:3]

참가 물질

5

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온도
0 °C

실험 절차

To a stirred solution of 2-allyloxy-ethanol 7 (10.9 mL, 100 mmol, 1.0 equiv.) in THF (200 mL) was carefully added NaH (60%, 4.8 g, 120 mmol, 1.2 equiv.) in small portions at room temperature. The reaction was then refluxed for 1 h (until H2 release ceased) then cooled to 0° C. Methyl bromoacetate (11.4 mL, 120 mmol, 1.2 equiv.) was then added dropwise. After 15 min at 0° C., the reaction was submitted to a EtOAc/H2O extraction. The combined organic layers were washed with brine, dried over anhydrous MgSO4, filtered then evaporated under reduced pressure. Purification was achieved by Kugelrohr distillation under reduced pressure and provided 9.77 g (55%) of ester (8) as a colorless oil; bp=130-145° C. (water tap vacuum); 1H NMR (400 MHz, CDCl3) δ 5.91 (m, 1H), 5.28 (m, 1H), 4.99 (m, 1H), 4.19 (s, 2H), 4.02 (m, 2H), 3.76 (s, 3H), 3.75 (m, 2H), 3.64 (m, 2H); 13C NMR (100 MHz, CDCl3) δ 171.1, 134.8, 117.3, 72.4, 71.2, 69.7, 68.9, 51.9; IR (neat) 1755 cm−1; HRMS (ESI, m/z) calcd. for C8H15O4 (MH+) 175.0964, found 175.0960.

후처리

  1. customat room temperature
  2. temperatureThe reaction was then refluxed for 1 h (until H2 release ceased)
  3. extractionthe reaction was submitted to a EtOAc/H2O extraction
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over anhydrous MgSO4
  6. filtrationfiltered
  7. customthen evaporated under reduced pressure
  8. customPurification
  9. distillationwas achieved by Kugelrohr distillation under reduced pressure

출처 및 근거

ORD 기록
ord-50f84401601447bdbacc50e6c6307ef4
출처 데이터셋
uspto-grants-2015_07
특허 번호
US09078956B2

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