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Acetic Acid → HCID 15289937、化合物

HRID 1648225
ノート
印刷プレビュー

反応式

HRID 1648225 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

HCID 15289937HCID 15289937、化合物

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 1140Toluene溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-7d5d5fcfbbd14c2483863e1db169c0e3
出典データセット
uspto-grants-1995_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05436242

反応ノート

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