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Acetic Anhydride → 1-(3-Nitrophenyl)propan-2-one

HRID 1728540
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HRID 1728540 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH2:10][C:11]([OH:13])=O)[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[C:14](OC(=O)C)(=O)C>N1C=CC=CC=1>[N+:1]([C:4]1[CH:5]=[C:6]([CH2:10][C:11](=[O:13])[CH3:14])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2]
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참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 158763-Nitrophenylacetic acid

생성물 1

HCID 125079341-(3-Nitrophenyl)propan-2-one

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

A mixture of 3-nitrophenyl acetic acid (20 g), pyridine (44 g) and acetic anhydride (106 g) was refluxed for four hours. Complete disappearance of starting material was observed by tlc (silica gel eluted with 1:1 parts by volume diethyl ether:hexane), and the brown solution was then evaporated to dryness in vacuo at 40°. The resulting residue was refluxed in the presence of concentrated HCl (7.5 ml) and ethanol (78 ml) for one hour; and to the hydrolysis product was added ice water (400 ml) and the precipitating 3-nitrophenyl acetone was filtered and washed with water. Additional product was obtained by extracting the filtrate with methylene chloride, drying over sodium sulfate, and evaporating the organic solvents. The crude products were combined and dissolved in a minimum amount of methanol:methylene chloride (1:1 parts by volume). Silica gel (30-50 g, flash chromatography, EM 230-400 mesh) was added and the solvent evaporated. The dried silica gel was placed on a column (3 in.×6 in.) containing the same silica gel and eluted with 4:6 parts by volume ethyl acetate:hexane. The solution containing the desired product was evaporated to give the title compound. NMR for this product (in CDCl3) shows a 3 proton singlet at 2.34 ppm; a 2 proton singlet at 3.63 ppm; a 2 proton multiplet at 7.5 ppm; and a 2 proton multiplet at 8.0 ppm.

후처리

  1. temperaturewas refluxed for four hours
  2. washComplete disappearance of starting material was observed by tlc (silica gel eluted with 1:1 parts by volume diethyl ether:hexane)
  3. customthe brown solution was then evaporated to dryness in vacuo at 40°
  4. temperatureThe resulting residue was refluxed in the presence of concentrated HCl (7.5 ml) and ethanol (78 ml) for one hour
  5. additionand to the hydrolysis product was added ice water (400 ml)
  6. filtrationthe precipitating 3-nitrophenyl acetone was filtered
  7. washwashed with water
  8. customAdditional product was obtained
  9. extractionby extracting the filtrate with methylene chloride
  10. dry with materialdrying over sodium sulfate
  11. customevaporating the organic solvents
  12. dissolutiondissolved in a minimum amount of methanol:methylene chloride (1:1 parts by volume)
  13. additionSilica gel (30-50 g, flash chromatography, EM 230-400 mesh) was added
  14. customthe solvent evaporated
  15. additioncontaining the same silica gel
  16. washeluted with 4:6 parts by volume ethyl acetate
  17. additionThe solution containing the desired product
  18. customwas evaporated

출처 및 근거

ORD 기록
ord-09db227f874f401fa3eb13a757113929
출처 데이터셋
uspto-grants-1994_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05328828

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