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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Acid → HCID 15289937, 화합물

HRID 1648225
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HRID 1648225 반응식
C(O)(=[O:3])C.[F:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[CH:12]=[C:13]([N+]([O-])=O)[CH2:14][CH3:15]>[Zn].C1(C)C=CC=CC=1>[F:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[CH2:12][C:13](=[O:3])[CH2:14][CH3:15]
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참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 42261071-(2-Fluorophenyl)-2-nitro-1-butene

생성물 1

HCID 15289937HCID 15289937, 화합물

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 1140Toluene용매

실험 절차

100 ml of 90% v/v aqueous acetic acid were added to 7.4 g of 1-(2-fluorophenyl)-2-nitro-1-butene [prepared as described in step (a) above], and then 12.11 g (190 mmole) of a zinc powder were added in portions to the resulting solution, whilst heating. The mixture was then heated under reflux, whilst stirring, for 4 hours. At the end of this time, the reaction mixture was left to stand overnight, and then the crystals which had precipitated were filtered off and washed with toluene. The filtrate was combined with the toluene washings, and the mixture was concentrated by evaporation under reduced pressure. The residue thus obtained was subjected to silica gel column chromatography, using toluene as the eluent, to give 1.85 g of the title compound as a pale brown oil.

후처리

  1. temperaturewhilst heating
  2. temperatureThe mixture was then heated
  3. temperatureunder reflux
  4. waitAt the end of this time, the reaction mixture was left
  5. waitto stand overnight
  6. customthe crystals which had precipitated
  7. filtrationwere filtered off
  8. washwashed with toluene
  9. concentrationthe mixture was concentrated by evaporation under reduced pressure
  10. customThe residue thus obtained

출처 및 근거

ORD 기록
ord-7d5d5fcfbbd14c2483863e1db169c0e3
출처 데이터셋
uspto-grants-1995_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05436242

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