4-Fluoroiodobenzene → 1-(4-fluorophenyl)-3-(2-hydroxyethyl)-2(3H)-benzimidazolone

HRID 369770

Reaktionsgleichung

Reaktionsgleichung von HRID 369770
[OH:1][CH2:2][CH2:3][N:4]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[NH:6][C:5]1=[O:13].[F:14][C:15]1[CH:20]=[CH:19][C:18](I)=[CH:17][CH:16]=1.C(=O)([O-])[O-].[K+].[K+].[I-]>[O-2].[Zn+2].O>[F:14][C:15]1[CH:20]=[CH:19][C:18]([N:6]2[C:7]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[N:4]([CH2:3][CH2:2][OH:1])[C:5]2=[O:13])=[CH:17][CH:16]=1

Komponenten

7

Versuchsvorschrift

A mixture of 1-(2-hydroxyethyl)benzimidazolone (J. Davoll, J. Chem. Soc., 1960, 308) (9 g), 4-fluoroiodobenzene (23 g), potassium carbonate (8.0 g), cupper(I) iodide (1 g), and zinc oxide (0.5 g) in N-methyl-2(3H)-pyrrolidinone (100 ml) was kept at 155° C. for 4.5 h. After cooling water (500 ml) was added followed by extraction with ethyl acetate (3×200 ml). The organic phase was washed with water and saturated calcium chloride solution and dried over magnesium sulfate. Removal of solvent in vacuo gave an oil which was purified by chromatography (silica gel, ethyl acetate) giving 1-(4-fluorophenyl)-3-(2-hydroxyethyl)-2(3H)-benzimidazolone (2 g) as a solid, mp: 124-26° C.

Aufarbeitung

  1. additionwas added
  2. extractionfollowed by extraction with ethyl acetate (3×200 ml)
  3. washThe organic phase was washed with water and saturated calcium chloride solution
  4. dry with materialdried over magnesium sulfate
  5. customRemoval of solvent in vacuo
  6. customgave an oil which
  7. customwas purified by chromatography (silica gel, ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-0f596369f7ca41c9afacb3fc9db6f7c6
Quelldatensatz
uspto-grants-2000_10
Patentnummer
US06140331

Verknüpfte Notizen

Wird geladen…