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Hydrochloric Acid → 4-Methyl-2,3,5,6-tetrafluorobenzonitrile

HRID 1153713
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HRID 1153713 반응식
P(Cl)(Cl)(Cl)=O.[F:6][C:7]1[C:12]([F:13])=[C:11]([C:14]([NH2:16])=O)[C:10]([F:17])=[C:9]([F:18])[C:8]=1[CH3:19].Cl>C(Cl)Cl.N1C=CC=CC=1>[C:14]([C:11]1[C:10]([F:17])=[C:9]([F:18])[C:8]([CH3:19])=[C:7]([F:6])[C:12]=1[F:13])#[N:16]
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 24813Phosphorus oxychlorideHCID 204362822,3,5,6-Tetrafluoro-4-toluamide

생성물 1

HCID 117887354-Methyl-2,3,5,6-tetrafluorobenzonitrile

시약·촉매·용매 2

HCID 1049Pyridine용매HCID 6344Dichloromethane용매

실험 절차

A solution of phosphorus oxychloride (1.4 g) in methylene chloride (4 ml) was added slowly to a solution of 2,3,5,6-tetrafluoro-4-toluamide (1.0 g) in pyridine (8 ml) at -5° C. When the addition was complete the mixture was warmed to the ambient temperature over a period of 90 minutes, poured into a mixture of dilute hydrochloric acid and ice, and the resultant mixture was extracted with methylene chloride. After washing the extract with water (three times) and drying over anhydrous magnesium sulphate, the solvent was removed by evaporation under reduced pressure. The residual oil was purified by distillation under water pump pressure in a Kugelrohr apparatus to yield 4-cyano-2,3,5,6-tetrafluorotoluene, identified by infra red spectroscopy.

후처리

  1. additionWhen the addition
  2. extractionthe resultant mixture was extracted with methylene chloride
  3. washAfter washing the
  4. extractionextract with water (three times)
  5. dry with materialdrying over anhydrous magnesium sulphate
  6. customthe solvent was removed by evaporation under reduced pressure
  7. distillationThe residual oil was purified by distillation under water

출처 및 근거

ORD 기록
ord-eccec0ae257c4863a193df954b6def43
출처 데이터셋
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04486355

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