1,3-Dichloro-2-propanol → 1,3-Dichloro-2-propanol

HRID 2068446Notes

Reaction equation

HRID 2068446 reaction equation
[CH2:1]([CH:3]1[O:5][CH2:4]1)[Cl:2].[CH2:6]([Cl:11])[CH:7]([OH:10])[CH2:8][Cl:9]>O>[CH2:6]([Cl:11])[CH:7]([OH:10])[CH2:8][Cl:9].[OH2:5].[CH2:1]([CH:3]1[O:5][CH2:4]1)[Cl:2]

Participants

5

Procedure

British Patent Specification 974,164, for example, discloses a process and apparatus for the production of epichlorohydrin from dichlorohydrin in which an aqueous reaction medium comprising an inorganic alkali hydroxide, water and dichlorohydrin are mixed and then treated with steam in a reactor column at a temperature below 55° C. to strip epichlorohydrin formed by the reaction between the inorganic alkali hydroxide and dichlorohydrin from the reaction mixture as a gaseous water-epichlorohydrin azeotrope. The overhead is condensed and separated in a liquid-liquid phase separator into an aqueous phase, which is recycled to the dehydrochlorination reactor column, and an organic phase, which is fed to a drying column to remove epichlorohydrin and residual water as a vapor phase. The vapor phase is condensed and recycled to the liquid-liquid phase separator to remove residual water from the drying column.

Workup

  1. additionare mixed
  2. additiontreated with steam in a reactor column at a temperature below 55° C.

Sources & evidence

ORD record
ord-8c699cde1cd144f5a011271601981f1b
Source dataset
uspto-grants-2012_10
Patent number
US08298500B2

Reaction notes

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