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Diethyl Ether → Ethyl 3-(furan-3-yl)acrylate

HRID 611067
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HRID 611067 반응식
C(OP([CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])(OCC)=O)C.[H-].[Na+].[O:17]1[CH:21]=[CH:20][C:19]([CH:22]=O)=[CH:18]1.CCOCC>C1C=CC=CC=1>[O:17]1[CH:21]=[CH:20][C:19](/[CH:22]=[CH:9]/[C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:18]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 3283Diethyl EtherHCID 103513-FuraldehydeHCID 13345Triethyl phosphonoacetateHCID 24758Sodium hydride

생성물 1

HCID 10103508Ethyl 3-(furan-3-yl)acrylate

시약·촉매·용매 1

HCID 241Benzene용매2회

실험 절차

To a solution of 17.7 g (78.8 mmol) of ethyl diethylphosphonoacetate in 150 ml of benzene, 2.89 g (72.2 mmol) of sodium hydride (60% in oil) was added under ice-cooling, followed by stirring for 30 minutes. To this solution, a solution of 6.308 g (65.65 mmol) of 3-furaldehyde in 50 ml of benzene was added dropwise, followed by stirring at room temperature for 30 minutes and refluxing for 30 minutes. After the reaction mixture was cooled to room temperature, ether was added; the mixture was then washed with water. The ether solution was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (hexane to hexane/ethyl acetate=9/1) to yield the desired product.

후처리

  1. temperaturecooling
  2. stirringby stirring at room temperature for 30 minutes
  3. temperaturerefluxing for 30 minutes
  4. washthe mixture was then washed with water
  5. dry with materialThe ether solution was dried over anhydrous magnesium sulfate
  6. distillationthe solvent was distilled off under reduced pressure
  7. customThe resulting crude product was purified by silica gel column chromatography (hexane to hexane/ethyl acetate=9/1)

출처 및 근거

ORD 기록
ord-afe5c1d3b79a4e8193a80a8094624352
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05998433

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