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1-Iodohexane → Ethyl 2-Hexylhexan-3-onecarboxylate

HRID 1698848
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HRID 1698848 반응식
[Na].[CH2:2]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:3][C:4](=[O:8])[CH2:5][CH2:6][CH3:7].I[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]>C(O)C>[CH2:15]([CH:3]([C:4](=[O:8])[CH2:5][CH2:6][CH3:7])[CH2:2][C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:16][CH2:17][CH2:18][CH2:19][CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 125271-IodohexaneHCID 5360545SodiumHCID 12271529Ethyl 4-oxoheptanoate

생성물 1

HCID 18322309Ethyl 2-Hexylhexan-3-onecarboxylate

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Under an atmosphere of argon, 1.59 g (69.3 mmol) of sodium were added a little at a time to 50 ml of ethanol. The mixture was then stirred under reflux until a homogeneous solution was obtained. 11.0 g (69.3 mmol) of ethyl hexan-3-onecarboxylate were added to the hot alkoxide solution, and the mixture was stirred for 45 min. 6.51 ml (7.93 g, 52.5 mmol) of 1-iodohexane were then slowly added dropwise to the boiling mixture. The mixture was stirred under reflux for 16 h, cooled to room temperature and filtered, and the solvent was then removed under reduced pressure. The residue was taken up in dichloromethane, filtered again and concentrated. The crude product was purified chromatographically (silica gel, petroleum ether: ethyl acetate 30:1). MS (DCI, NH3): 309 [M+H]+.

후처리

  1. temperatureunder reflux until a homogeneous solution
  2. customwas obtained
  3. stirringthe mixture was stirred for 45 min
  4. stirringThe mixture was stirred
  5. temperatureunder reflux for 16 h
  6. filtrationfiltered
  7. customthe solvent was then removed under reduced pressure
  8. filtrationfiltered again
  9. concentrationconcentrated
  10. customThe crude product was purified chromatographically (silica gel, petroleum ether: ethyl acetate 30:1)

출처 및 근거

ORD 기록
ord-87c4977085664f4eb1367e5b4ca68c2a
출처 데이터셋
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06344471B1

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