Water → (+/-)(1r,2r)-2-[(2z)-2-Pentenyl]-3-hydroxycyclopentaneethanol

HRID 1912228

반응식

HRID 1912228 반응식
[CH3:1][CH2:2]/[CH:3]=[CH:4]\[CH2:5][C@H:6]1[C:10](=[O:11])[CH2:9][CH2:8][C@@H:7]1[CH2:12][C:13](O)=[O:14].[H-].[Al+3].[Li+].[H-].[H-].[H-].O>O1CCCC1>[CH2:5]([C@H:6]1[CH:10]([OH:11])[CH2:9][CH2:8][C@@H:7]1[CH2:12][CH2:13][OH:14])/[CH:4]=[CH:3]\[CH2:2][CH3:1]

참가 물질

5

반응 조건

온도
50 °C

실험 절차

In a 50 ml three-necked flask equipped with a condenser, a thermometer and a magnetic stirrer, 1 g (4.5 mmol) of methyl (+/−)-jasmonate was dissolved in 15 ml of tetrahydrofuran. 430 mg (11.3 mmol) of lithium aluminium hydride, LiAlH4, were added. The mixture was stirred at 50° C. for 4 hours. When the reaction was finished, 5 ml of water were added slowly. The precipitate formed was filtered off and the filtrate was acidified to pH=5 with hydrochloric acid and then extracted with ethyl acetate (3×30 ml). The organic phase was dried over sodium sulphate, filtered on filter paper, and then concentrated. The colourless oil obtained was purified by chromatography on silica gel (eluent: dichloromethane/methanol). The colourless oil obtained was dried under vacuum.

후처리

  1. customIn a 50 ml three-necked flask equipped with a condenser
  2. customThe precipitate formed
  3. filtrationwas filtered off
  4. extractionextracted with ethyl acetate (3×30 ml)
  5. dry with materialThe organic phase was dried over sodium sulphate
  6. filtrationfiltered
  7. filtrationon filter paper
  8. concentrationconcentrated
  9. customThe colourless oil obtained
  10. customwas purified by chromatography on silica gel (eluent: dichloromethane/methanol)
  11. customThe colourless oil obtained
  12. customwas dried under vacuum

출처 및 근거

ORD 기록
ord-15fc593b8ae54be6b7b06bfe6d9c1c7b
출처 데이터셋
uspto-grants-2013_12
특허 번호
US08609117B2

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