Iodine → HCID 20470550, Verbindung

HRID 1388243Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1388243
[CH3:1][O:2][CH2:3][CH2:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:7][CH:6]=1.[I:17](O)(=O)=O.II.S(=O)(=O)(O)O.S([O-])([O-])(=O)=S.[Na+].[Na+]>C(Cl)(Cl)(Cl)Cl.O.C(O)(=O)C>[CH3:1][O:2][CH2:3][CH2:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][C:14]([I:17])=[CH:13][CH:12]=2)=[CH:7][CH:6]=1

Komponenten

9

Reaktionsbedingungen

Temperatur
83 °C

Versuchsvorschrift

Into a 300 ml three-neck flask were added 4-(β-methyloxyethyl) biphenyl (34 g, 0.16 mol), acetic acid (112 ml), water (30 ml), iodic acid (6.8 g, 0.0384 mol), iodine (17.9 g, 0.0704 mol), carbon tetrachloride (13 ml) and conc. sulfuric acid (4.8 ml). The mixture was warmed by a mantle heater with stirring, and reaction was carried out under reflux at 83° C. for 3 hours. After completion of the reaction, the reaction liquid was cooled down to 70° C., and 10% sodium thiosulfate aqueous solution (10 ml) was added to cause excess iodine to disappear. The liquid was cooled down to room temperature, and the precipitated crystals were recrystallized from ethyl ethanol (300 ml) to obtain 4'-(β-methoxyethyl)-4-iodobiphenyl (V) (30 g) having a melting point of 97°~99.4° C.

Aufarbeitung

  1. temperatureThe mixture was warmed by a mantle heater
  2. customreaction
  3. customAfter completion of the reaction
  4. customthe reaction liquid
  5. temperaturewas cooled down to 70° C.
  6. temperatureThe liquid was cooled down to room temperature
  7. customthe precipitated crystals were recrystallized from ethyl ethanol (300 ml)

Quellen und Nachweise

ORD-Eintrag
ord-dca8434e973242e29f4406eec8532ad8
Quelldatensatz
uspto-grants-1984_02
Patentnummer
US04431564

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