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2-Methoxyethanol → Methoxyethoxy-(3e)-1,3-pentadiene

HRID 991253
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HRID 991253 반응식
[Na].Br[CH2:3]/[CH:4]=[CH:5]/[CH:6]=[CH2:7].[CH3:8][O:9][CH2:10][CH2:11][OH:12]>>[CH3:8][O:9][CH2:10][CH2:11][O:12][CH:7]=[CH:6]/[CH:5]=[CH:4]/[CH3:3]
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참가 물질

4

반응물 3

HCID 80192-MethoxyethanolHCID 5360545SodiumHCID 5365559(3E)-5-Bromo-1,3-pentadiene

생성물 1

HCID 131723540Methoxyethoxy-(3e)-1,3-pentadiene수율 75%

실험 절차

Under a nitrogen atmosphere, to a stirred solution of sodium (0.53 g, 23 mmol) in 2-methoxyethanol (50 mL) at room temperature was added 5-bromo-(3E)-1,3-pentadiene (3.38 g, 23 mmol). The mixture was stirred overnight and then refluxed for three more hours. Excess 2-methoxyethanol was removed by distillation. Water was added to the cooled reaction mixture, which was then extracted with diethyl ether. The diethyl ether solution was dried over MgSO4, then stripped off at reduced pressure. Distillation at 87-88° C., 31 mmHg (water aspirator) yielded 2.46 g (75%) of the desired compound.

후처리

  1. temperaturerefluxed for three more hours
  2. customExcess 2-methoxyethanol was removed by distillation
  3. additionWater was added to the cooled reaction mixture, which
  4. extractionwas then extracted with diethyl ether
  5. dry with materialThe diethyl ether solution was dried over MgSO4
  6. distillationDistillation at 87-88° C.

출처 및 근거

ORD 기록
ord-6e059a2bf50c41c48ba8f2be35d870b1
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06462207B1

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