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Acetic Acid → N-(4-Fluorobenzylidene)aniline

HRID 1492657
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인쇄 미리보기

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HRID 1492657 반응식
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[NH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C1C=CC=CC=1.C(O)(=O)C>O>[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[N:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 241BenzeneHCID 6115AnilineHCID 680234-Fluorobenzaldehyde

생성물 1

HCID 918392N-(4-Fluorobenzylidene)aniline

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To 4-fluorobenzaldehyde (24.8 g, 0.200 mol) and aniline (18.6 g, 0.200 mol) was added benzene (200 mL) and acetic acid (0.7 mL) and the mixture is heated under reflux until all the water (3.6 mL) was azeotropically removed. The solvent is evaporated and the residual oil upon cooling and stirring crystallized. The white mass was then recrystallized as needles (28 g, 70%): mp 39°-40° C. (PE) (lit.1 mp 40° C.).

후처리

  1. temperaturethe mixture is heated
  2. customwas azeotropically removed
  3. customThe solvent is evaporated
  4. temperaturethe residual oil upon cooling
  5. customcrystallized
  6. customThe white mass was then recrystallized as needles (28 g, 70%)

출처 및 근거

ORD 기록
ord-fa25214b4cea40cab83e37faa36aecfd
출처 데이터셋
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05374701

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