Allyl bromide → Methyl 2-(allyloxy)propanoate

HRID 242017

반응식

HRID 242017 반응식
[CH3:1][O:2][C:3](=[O:7])[CH:4]([OH:6])[CH3:5].[H-].[Na+].[CH2:10](Br)[CH:11]=[CH2:12].C(=O)(O)[O-].[Na+]>O1CCCC1.O>[CH2:12]([O:6][CH:4]([CH3:5])[C:3]([O:2][CH3:1])=[O:7])[CH:11]=[CH2:10]

참가 물질

7

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온도
0 °C

실험 절차

(±)-Methyl-2-hydroxypropanoate (7.6 g, 74 mmol) was dissolved in tetrahydrofuran (100 mL), cooled to 0° C. and treated with sodium hydride (3.6 g, 60% dispersion, 89 mmol, 1.2 equiv) portionwise over 45 minutes. The mixture was warmed to ambient temperature, stirred for 30 minutes, and then cooled to 0° C. Allyl bromide (8.4 mL, 96 mmol, 1.3 equiv) was added, the mixture was warmed to ambient temperature and stirred for an additional 14 hours. Sodium bicarbonate (10 mL, aqueous saturated) was added slowly and the mixture was stirred for 30 minutes before being poured into water (500 mL). The aqueous layer was extracted with ethyl acetate (2×300 mL) and the combined organic extracts were washed once with brine, dried with sodium sulfate, filtered and concentrated in vacuo, providing the titled compound.

후처리

  1. temperatureThe mixture was warmed to ambient temperature
  2. temperaturecooled to 0° C
  3. temperaturethe mixture was warmed to ambient temperature
  4. stirringstirred for an additional 14 hours
  5. stirringthe mixture was stirred for 30 minutes
  6. extractionThe aqueous layer was extracted with ethyl acetate (2×300 mL)
  7. washthe combined organic extracts were washed once with brine
  8. dry with materialdried with sodium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-d4ecf825aa5b4d4e89202ad8f730cded
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08653079B2

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