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Acetic Acid → HCID 53915788, 화합물

HRID 1350117
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HRID 1350117 반응식
C(O)(=O)C.[N:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11](=[N:20]O)[CH2:12][CH2:13][CH:14]2[CH2:19][CH2:18][O:17][CH2:16][CH2:15]2)[CH:6]=1>C(O)C.[Zn]>[N:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH:11]([NH2:20])[CH2:12][CH2:13][CH:14]2[CH2:15][CH2:16][O:17][CH2:18][CH2:19]2)[CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 85974475HCID 85974475, 화합물

생성물 1

HCID 53915788HCID 53915788, 화합물수율 93%

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 702Ethanol용매

실험 절차

Acetic acid (16 mL) was added to a suspension of 1-(3-pyridyl)-3-(4-oxanyl)propan-1-one oxime (1.60 g, 6.83 mmol) in 95% ethanol (40 mL) over a period of 15 min. Zinc dust (12 g, 180 mmol) was added and the reaction mixture was stirred at ambient temperature for 4 h. The reaction mixture was filtered through a Celite plug, which was then washed with ethanol (50 mL). The combined filtrates were concentrated by rotary evaporation. The solid residue was made basic by addition of 50% aqueous NaOH (with ice bath cooling), saturated with solid NaCl and extracted with chloroform (5×30 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated by rotary evaporation to give pure product as a colorless viscous liquid (1.40 g, 82% yield).

후처리

  1. filtrationThe reaction mixture was filtered through a Celite plug, which
  2. washwas then washed with ethanol (50 mL)
  3. concentrationThe combined filtrates were concentrated by rotary evaporation
  4. additionThe solid residue was made basic by addition of 50% aqueous NaOH (with ice bath cooling), saturated with solid NaCl
  5. extractionextracted with chloroform (5×30 mL)
  6. dry with materialThe combined organic extracts were dried (Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated by rotary evaporation

출처 및 근거

ORD 기록
ord-a0cd146571e84fbcb0c2bdd61563b1be
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07214686B2

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