Hydrochloric Acid → 1,1-Dichloroethane

HRID 643052

Reaktionsgleichung

Reaktionsgleichung von HRID 643052
[Cl:1][CH:2]([Cl:4])[CH3:3].[FH:5].[F:6][CH:7]([F:9])[CH3:8].Cl>[O-2].[Cr+3].[O-2].[O-2].[Cr+3]>[F:6][CH:7]([F:9])[CH3:8].[FH:5].[Cl:1][CH:2]([Cl:4])[CH3:3].[Cl:1][CH:2]([F:6])[CH3:3]

Komponenten

9

Versuchsvorschrift

1,1-Dichloroethane and hydrogen fluoride were introduced into an inconel-made reactor filled with a catalyst (mainly comprising trivalent chromium oxide) and reacted at a reaction temperature of 250° C., the resulting reaction gas, mainly comprising 1,1-difluoroethane, hydrogen chloride and unreacted hydrogen fluoride, was introduced into a first distillation tower, hydrogen chloride which is a low boiling fraction was mainly separated from the top, and hydrogen fluoride, 1,1-difluoroethane, 1,1-dichloroethane and 1-chloro-1-fluoroethane were mainly separated from the bottom and introduced into a second distillation tower. In the second distillation tower, crude 1,1-difluoroethane mainly comprising 1,1-difluoroethane was obtained from the top and hydrogen fluoride, 1,1-dichloroethane and 1-chloro-fluoroethane were mainly separated from the bottom and recirculated to the above-described reaction step. The obtained crude 1,1-difluoroethane had the following composition.

Aufarbeitung

  1. customreacted at a reaction temperature of 250° C.
  2. customwas mainly separated from the top, and hydrogen fluoride, 1,1-difluoroethane, 1,1-dichloroethane and 1-chloro-1-fluoroethane
  3. customwere mainly separated from the bottom and
  4. additionintroduced into a second distillation tower

Quellen und Nachweise

ORD-Eintrag
ord-74034e474fee411a9c9ba94262a0b2c1
Quelldatensatz
uspto-grants-2010_04
Patentnummer
US07696392B2

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