1,1-Dichloropropane → 1,1,2-Trichloropropane

HRID 522495

Reaktionsgleichung

Reaktionsgleichung von HRID 522495
[CH3:1][CH2:2][CH:3]([Cl:5])[Cl:4].C1C([Cl:12])=C(Cl)C=C(Cl)C=1OCCO.C1C=C[NH+]=CC=1.C1C=C[NH+]=CC=1.[O-][Cr](O[Cr]([O-])(=O)=O)(=O)=O>>[Cl:4][CH:3]([Cl:5])[CH:2]([Cl:12])[CH3:1].[Cl:4][C:3]([Cl:12])([Cl:5])[CH2:2][CH3:1]

Komponenten

5

Versuchsvorschrift

In the present process, dichloropropane is converted to a chlorinated alkene, e.g., TCPE, using a series of consecutive chlorination and dehydrochlorination steps. In one exemplary embodiment, PDC is fed to a liquid phase chlorination reactor, e.g., such as a batch or continuous stirred tank autoclave reactor with an internal cooling coil. A shell and multitube exchanger operating in plug flow, followed by vapor liquid disengagement tank or vessel can also be used. Suitable reaction conditions include, e.g., a temperature of from 30° C. to 150° C., a pressure of from 100 kPa to 2000 kPa. The reaction is carried out in the presence of one or more regioselective catalysts that provide a regioselectivity to, e.g., 1,1,2-trichloropropane of at least 5:1 over other trichloropropane isomers.

Aufarbeitung

  1. customSuitable reaction conditions
  2. customof from 30° C. to 150° C.

Quellen und Nachweise

ORD-Eintrag
ord-14b2e5b709964b72bcc0c865ee0479e2
Quelldatensatz
uspto-grants-2016_05
Patentnummer
US09334205B2

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