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Hydrochloric Acid → 5-Methoxy-1-phenyl-1-pentanone

HRID 975254
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HRID 975254 반응식
[C:1]1([Mg]Br)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:9][O:10][CH:11](C)[CH2:12][CH2:13][CH2:14][C:15]#N.Cl.C([O:21]CC)C>>[CH3:9][O:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)=[O:21]
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참가 물질

5

반응물 4

HCID 313Hydrochloric AcidHCID 3283Diethyl Ether2회HCID 19971645HCID 19971645, 화합물HCID 178418255HCID 178418255, 화합물

생성물 1

HCID 119662825-Methoxy-1-phenyl-1-pentanone

실험 절차

To a solution of phenylmagnesium bromide (16.0 g, 88 mmol) in anhydrous diethylether (55 ml) under an atmosphere of nitrogen was dropwise added a solution of the above nitrile (10.0 g, 88 mmol) in anhydrous diethylether while the temperature was allowed to raise to reflux. The reaction mixture was heated at reflux for 5 h and then stirred at room temperature for 16 h. A 4N hydrochloric acid solution (50 ml) was carefully added and the mixture stirred at ambient temperature for 4 h. The phases were separated and the aqueous phase extracted with diethylether (2×50 ml). The combined organic phases were washed with 5% sodium hydrogencarbonate (25 ml) and dried (Na2SO4). The solvent was evaporated in vacuo and the residue submitted to fractional distillation to give 9.1 g of 5-methoxy-1-phenyl-1-pentanone. B.p. 127°-130° C./5 mmHg.

후처리

  1. temperatureto raise
  2. temperatureto reflux
  3. temperatureThe reaction mixture was heated
  4. temperatureat reflux for 5 h
  5. stirringthe mixture stirred at ambient temperature for 4 h
  6. customThe phases were separated
  7. extractionthe aqueous phase extracted with diethylether (2×50 ml)
  8. washThe combined organic phases were washed with 5% sodium hydrogencarbonate (25 ml)
  9. dry with materialdried (Na2SO4)
  10. customThe solvent was evaporated in vacuo
  11. distillationthe residue submitted to fractional distillation

출처 및 근거

ORD 기록
ord-c1845af3ab2e46ef885e81c66d419c0c
출처 데이터셋
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05608069

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