Cyclopentadiene → 5-(Pentan-2-ylidene)cyclopenta-1,3-diene

HRID 495748노트

반응식

HRID 495748 반응식
[CH:1]1[CH2:5][CH:4]=[CH:3][CH:2]=1.[CH2:6]([C:9]([CH3:11])=O)[CH2:7][CH3:8].N1CCCC1>CO.CCOCC.O>[CH3:8][C:7]([CH2:6][CH2:9][CH3:11])=[C:2]1[CH:1]=[CH:5][CH:4]=[CH:3]1

참가 물질

7

반응물 3

HCID 7612CyclopentadieneHCID 78952-PentanoneHCID 31268Pyrrolidine

생성물 1

HCID 129395315-(Pentan-2-ylidene)cyclopenta-1,3-diene수율 61%

시약·촉매·용매 3

HCID 887Methanol용매HCID 962Water용매HCID 3283Diethyl Ether용매

실험 절차

To a solution of 10.00 g (151.3 mmol) of cyclo pentadiene in 40 ml of methanol, 18.6 ml (174.2 mmol) of methyl propyl ketone and 4.5 ml (54.7 mmol) of pyrrolidine were added with ice cooling, followed by stirring at room temperature for one night. After the reaction solution was diluted with 100 ml of ether, 50 ml of water was added. The organic phase was separated, washed with water and a saturated saline solution, then dried over anhydrous magnesium sulfate and filtered. From the filtrate, the solvent was removed under reduced pressure to obtain a liquid. The liquid was subjected to vacuum distillation (70° C./1 mmHg) to obtain 12.30 g (91.64 mmol) of a yellow liquid (yield: 61%). The analyzed values are given below.

후처리

  1. additionwas added
  2. customThe organic phase was separated
  3. washwashed with water
  4. dry with materiala saturated saline solution, then dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. customFrom the filtrate, the solvent was removed under reduced pressure
  7. customto obtain a liquid
  8. distillationThe liquid was subjected to vacuum distillation (70° C./1 mmHg)

출처 및 근거

ORD 기록
ord-8b87efa02d214fadb553874996037d50
출처 데이터셋
uspto-grants-2005_09
특허 번호
US06939928B1

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