Iodine → HCID 13338730, Verbindung

HRID 2417846Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2417846
[NH:1]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][C:2]1=[O:14].P(Cl)(Cl)(Cl)(Cl)Cl.II.[Br:23]Br>C(Cl)(Cl)Cl>[Br:23][CH:3]1[CH2:4][CH2:5][CH2:6][CH2:7][C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[NH:1][C:2]1=[O:14]

Komponenten

6

Versuchsvorschrift

To a solution of 1,3,4,5,6,7-hexahydro-1-benzazonin-2-one (4.7 g) in chloroform (75 ml), phosphorus pentachloride (5.9 g) is added in portions, while maintaining the temperature at 0°-5° C. When addition is complete, iodine (60 mg) is added, followed by bromine (4.5 g), which is added dropwise over five minutes. The mixture is then refluxed for 4 hours. The chloroform solution is evaporated and the residue partitioned between ice/water (60 ml) and dichloromethane (100 ml). The organic phase is dried over magnesium sulfate and evaporated under reduced pressure. The crude residue is purified by chromatography on silica gel, eluting with ether/hexane mixtures. Concentration of the appropriate fractions yields 3-bromo-1,3,4,5,6,7-hexahydro-1-benzazonin-2-one.

Aufarbeitung

  1. temperaturewhile maintaining the temperature at 0°-5° C
  2. additionWhen addition
  3. additionis added dropwise over five minutes
  4. temperatureThe mixture is then refluxed for 4 hours
  5. customThe chloroform solution is evaporated
  6. customthe residue partitioned between ice/water (60 ml) and dichloromethane (100 ml)
  7. dry with materialThe organic phase is dried over magnesium sulfate
  8. customevaporated under reduced pressure
  9. customThe crude residue is purified by chromatography on silica gel
  10. washeluting with ether/hexane mixtures

Quellen und Nachweise

ORD-Eintrag
ord-c69dc7f1ab5242db90ed67aaae708e31
Quelldatensatz
uspto-grants-1984_09
Patentnummer
US04470988

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