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Potassium Hydroxide → Ethyl 2-benzylacrylate

HRID 36744
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HRID 36744 반응식
[OH-].[K+].[CH2:3]([O:5][C:6](=[O:20])[CH:7]([CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:8](OCC)=O)[CH3:4]>C(O)C>[CH2:8]=[C:7]([CH2:13][C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1)[C:6]([O:5][CH2:3][CH3:4])=[O:20]
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참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 69090Diethyl 2-benzylpropanedioate

생성물 1

HCID 11084648Ethyl 2-benzylacrylate수율 85.5%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

A mixture of KOH (8.5 g) in ethanol (100 mL) was added at room temperature to benzylmalonic acid diethyl ester (40 g) in ethanol (80 mL) and the whole was stirred at room temperature overnight, then concentrated by evaporation, thereafter water (14 mL) was added and then the mixture was acidified in an ice bath with concentrated hydrochloric acid (12.6 mL). Partitioning between water and ether was carried out, the organic phase was dried and the ether was distilled off. Then, pyridine (26 mL), piperidine (1.22 g) and paraformaldehyde (3.56 g) were added to the residue. The mixture was heated in an oil bath (130° ) for 90 minutes, cooled, water (440 mL) were added and extraction was carried out 3 times with n-hexane (150 mL). The combined organic phases were washed with water, 1N HCl, water, saturated NaHCO3 solution and brine. The solution was dried (MgSO4) and evaporated to give the title compound as colourless oil (26 g, 85% yield). 1H NMR: 300 MHz spectrum consistent with proposed structure.

후처리

  1. concentrationconcentrated by evaporation
  2. additionwater (14 mL) was added
  3. customthe mixture was acidified in an ice bath with concentrated hydrochloric acid (12.6 mL)
  4. customPartitioning between water and ether
  5. customthe organic phase was dried
  6. distillationthe ether was distilled off
  7. additionThen, pyridine (26 mL), piperidine (1.22 g) and paraformaldehyde (3.56 g) were added to the residue
  8. temperatureThe mixture was heated in an oil bath (130° ) for 90 minutes
  9. temperaturecooled
  10. additionwater (440 mL) were added
  11. extractionextraction
  12. washThe combined organic phases were washed with water, 1N HCl, water, saturated NaHCO3 solution and brine
  13. dry with materialThe solution was dried (MgSO4)
  14. customevaporated

출처 및 근거

ORD 기록
ord-49234da53e6a40af95a400d09ad649e8
출처 데이터셋
uspto-grants-1995_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05416119

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