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Ethanol → HCID 10426327, 화합물

HRID 1607666
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HRID 1607666 반응식
[F:1][C:2]1[CH:20]=[C:19]([F:21])[CH:18]=[CH:17][C:3]=1[O:4][C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][C:13]=1[N+:14]([O-:16])=[O:15])[C:8]([OH:10])=[O:9].[CH2:22](O)[CH3:23]>S(=O)(=O)(O)O>[F:1][C:2]1[CH:20]=[C:19]([F:21])[CH:18]=[CH:17][C:3]=1[O:4][C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][C:13]=1[N+:14]([O-:16])=[O:15])[C:8]([O:10][CH2:22][CH3:23])=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 702EthanolHCID 10402218HCID 10402218, 화합물

생성물 1

HCID 10426327HCID 10426327, 화합물

시약·촉매·용매 1

HCID 1118Sulfuric Acid촉매

실험 절차

A mixture of 3-(2,4-difluorophenoxy)-4-nitrobenzoic acid (1.0 g) and sulfuric acid (3 drops) in ethanol (5 ml) was refluxed for 8 hours. Ethanol was evaporated under reduced pressure, and the residue was dissolved in ethyl acetate, washed with a saturated aqueous solution of sodium bicarbonate, dried over magnesium sulfate, and concentrated to give pale brown needles of ethyl 3-(2,4-difluorophenoxy)-4-nitrobenzoate (1.1 g).

후처리

  1. temperature
was refluxed for 8 hours
  • customEthanol was evaporated under reduced pressure
  • dissolutionthe residue was dissolved in ethyl acetate
  • washwashed with a saturated aqueous solution of sodium bicarbonate
  • dry with materialdried over magnesium sulfate
  • concentrationconcentrated
  • 출처 및 근거

    ORD 기록
    ord-105ee1a6c2be4e77a071b7db2af7cbfa
    출처 데이터셋
    uspto-grants-1989_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04866091

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