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1-(3-Butenyl)Cyclopentane Carboxylic Acid Methyl Ester → HCID 86677562, 화합물

HRID 2401091
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HRID 2401091 반응식
[CH3:1][O:2][C:3]([C:5]1([CH2:10][CH2:11][CH:12]=C)[CH2:9][CH2:8][CH2:7][CH2:6]1)=[O:4].I([O-])(=O)(=O)=[O:15].[Na+]>C(O)(C)C.O.[Os](=O)(=O)(=O)=O>[CH3:1][O:2][C:3]([C:5]1([CH2:10][CH2:11][CH:12]=[O:15])[CH2:9][CH2:8][CH2:7][CH2:6]1)=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 233841621-(3-Butenyl)Cyclopentane Carboxylic Acid Methyl EsterHCID 23667635Sodium periodate

생성물 1

HCID 86677562HCID 86677562, 화합물

시약·촉매·용매 3

HCID 30318Osmium Tetroxide촉매HCID 962Water용매2회HCID 3776Isopropanol용매2회

실험 절차

To a solution of 1-but-3-enyl-cyclopentanecarboxylic acid methyl ester (4.0 g, 21.5 mmol) in isopropanol (35 mL) was added a solution of sodium periodate (10.1 g, 47.3 mmol) in H2O (35 mL) followed by the addition of osmium tetroxide (16 mg, 0.065 mmol). More isopropanol (30 mL) and H2O (35 mL) were added and the resulting suspension was stirred for 24 hours and then poured onto ice/H2O (200 mL) and extracted with EtOAc (2×200 mL). The organic layers were combined and dried over Na2SO4, filtered and concentrated to provide a crude oil which was purified by flash column chromatography (10 to 60% EtOAc/heptane) to provide 2.27 g (57 yield over two steps) of the title compound as an oil.

후처리

  1. additionpoured onto ice/H2O (200 mL)
  2. extractionextracted with EtOAc (2×200 mL)
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customto provide a crude oil which
  7. customwas purified by flash column chromatography (10 to 60% EtOAc/heptane)
  8. customto provide

출처 및 근거

ORD 기록
ord-e93137b2f41d4905bbc0272e54ff0219
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08796278B2

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