Chloride → 4-Chlorobenzene-1,2-dicarbonyl dichloride

HRID 2253874

Reaktionsgleichung

Reaktionsgleichung von HRID 2253874
[Cl-].BrBr.[Cl:4][CH:5]1[CH:13]=[CH:12][CH:8]([C:9]([Cl:11])=[O:10])[CH:7]([C:14]([Cl:16])=[O:15])[CH2:6]1>ClC1C=CC=CC=1>[Cl:4][C:5]1[CH:6]=[C:7]([C:14]([Cl:16])=[O:15])[C:8](=[CH:12][CH:13]=1)[C:9]([Cl:11])=[O:10]

Komponenten

5

Reaktionsbedingungen

Temperatur
135 °C

Versuchsvorschrift

To a 1--1 three-necked flask, equipped with a mechanical stirrer, a condenser with a gas outlet and an equa-pressured addition funnel, is charged 241.5 g (1 mole) of 4-chloratetrahydrophthaloyl chloride and 36 g of chlorobenzene. The mixture is heated to 100°-110° C. with stirring. Bromine, 320 g (2 moles) is added dropwise into the solution in a sub-surface manner. The color dissipates quickly and an evolution of gas occurs. When approximately 240 g of bromine has been added, the pot temperature is raised to 135° C. The addition of bromine continues until completion. The pot temperature is then raised to 165°-170° C. for 2-4 fours. During this period, an additional amount of bromine, such as about 10 to 15 g, may be added to complete the conversion of 4-chlorotetrahydrophthaloyl chloride. A good yield of 4-chlorophthaloyl chloride will be obtained from the distillation of the mixture.

Aufarbeitung

  1. customTo a 1--1 three-necked flask, equipped with a mechanical stirrer, a condenser with a gas outlet and an equa-pressured addition funnel
  2. temperatureThe mixture is heated to 100°-110° C.
  3. temperatureThe pot temperature is then raised to 165°-170° C. for 2-4 fours
  4. waitDuring this period

Quellen und Nachweise

ORD-Eintrag
ord-0ec1e0b8efd1492c8e79316137441980
Quelldatensatz
uspto-grants-1993_08
Patentnummer
US05233054

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