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4-Fluoroaniline → 2-(4'Fluorophenyl) aminocyclohex-1-ene-1-carbonitrile

HRID 366400
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반응식

HRID 366400 반응식
[F:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.O=[C:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH:11]1[C:16]#[N:17].[Cl-].[Ca+2].[Cl-]>>[F:1][C:2]1[CH:8]=[CH:7][C:5]([NH:6][C:10]2[CH2:15][CH2:14][CH2:13][CH2:12][C:11]=2[C:16]#[N:17])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 97314-FluoroanilineHCID 2202972-OxocyclohexanecarbonitrileHCID 5284359Calcium Chloride

생성물 1

HCID 702554742-(4'Fluorophenyl) aminocyclohex-1-ene-1-carbonitrile

실험 절차

4-Fluoro-aniline (1.11 g, 10.0 mmol), cyano-ketone (Example 32) (1.25 g, 10.2 mmol), calcium chloride (1.5 g, 13.5 mmol) and T.H.F. (20 ml) were heated under reflux for 17 hours. After cooling, the mixture was filtered and the solvent evaporated. Kugelrohr distillation (135° C., 0.08 mmHg) gave the product as a pale yellow powder.

후처리

  1. temperature(20 ml) were heated
  2. temperatureunder reflux for 17 hours
  3. temperatureAfter cooling
  4. filtrationthe mixture was filtered
  5. customthe solvent evaporated
  6. distillationKugelrohr distillation (135° C., 0.08 mmHg)

출처 및 근거

ORD 기록
ord-686a9c224c1149408ed9747acb345109
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06130228

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