Trifluoroacetic acid → 1,1-Di(p-fluorophenyl)urea

HRID 1589263Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1589263
[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=2)=[CH:4][CH:3]=1.[O:16]([C:18]#[N:19])[Na].C(C(O)=O)(F)(F)F>C(Cl)Cl.O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]([C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=2)[C:18]([NH2:19])=[O:16])=[CH:4][CH:3]=1

Komponenten

6

Edukt 3

HCID 6422Trifluoroacetic acidHCID 112411734-Fluoro-N-(4-fluorophenyl)benzenamineHCID 178418852HCID 178418852, Verbindung

Produkt 1

HCID 133624301,1-Di(p-fluorophenyl)urea

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

Di(p-fluorophenyl)amine (102.5 g., 0.5 mole) and NaOCN (65 g, 1.0 mole) were stirred in 700 ml CH2Cl2 at 16° C. F3CCOOH (84.5 ml, 117 g, 1.025 mole) was added as a thin stream over 5 minutes, during which the reaction mixture exothermed to 28° C. The exotherm peaked at 32° C. shortly after addition was complete. The reaction mixture was stirred at 23°-25° for 21 hours, diluted with 350 ml H2O and stirred 0.5 hour. The organic layer was separated and stirred 0.25 hour with 40 g NaOH in 500 ml H2O. The layers were separated, and the aqueous layer back washed with 100 ml CH2Cl2. The combined organic layer and back wash was dried (MgSO4), concentrated to 600 ml, diluted with 600 ml isopropanol, reconcentrated to 600 ml, rediluted with 600 ml of fresh isopropanol, reconcentrated to 800 ml, rediluted with 400 ml fresh isopropanol and again reconcentrated to 800 ml. The mixture was cooled to room temperature (product began to crystallize) and then to 0°-5° C. Title product was recovered by filtration, 104.9 g, m.p. 150°-153° C.

Aufarbeitung

  1. customexothermed to 28° C
  2. custompeaked at 32° C.
  3. additionshortly after addition
  4. stirringstirred 0.5 hour
  5. customThe organic layer was separated
  6. stirringstirred 0.25 hour with 40 g NaOH in 500 ml H2O
  7. customThe layers were separated
  8. washthe aqueous layer back washed with 100 ml CH2Cl2
  9. washThe combined organic layer and back wash
  10. dry with materialwas dried (MgSO4)
  11. concentrationconcentrated to 600 ml
  12. additiondiluted with 600 ml isopropanol
  13. additionrediluted with 600 ml of fresh isopropanol
  14. additionrediluted with 400 ml fresh isopropanol
  15. custom(product began to crystallize)
  16. customto 0°-5° C
  17. filtrationTitle product was recovered by filtration, 104.9 g, m.p. 150°-153° C.

Quellen und Nachweise

ORD-Eintrag
ord-ebe7dc976381433192a5bfa7838010b5
Quelldatensatz
uspto-grants-1986_02
Patentnummer
US04568748

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