Methyl 2,2,3,3,4,4,4-heptafluorobutanoate → Water methylheptafluorobutyrate

HRID 263324

Reaction equation

HRID 263324 reaction equation
[CH3:1][O:2][C:3](=[O:14])[C:4]([F:13])([F:12])[C:5]([F:11])([F:10])[C:6]([F:9])([F:8])[F:7]>O>[OH2:2].[CH3:1][O:2][C:3](=[O:14])[C:4]([F:12])([F:13])[C:5]([F:10])([F:11])[C:6]([F:8])([F:7])[F:9]

Participants

3

Procedure

Where desired, a mixture of water and methylheptafluorobutyrate can be distilled to produce an overhead water/methylheptafluorobutyrate azeotrope. This can be condensed and sufficiently highly cooled to cause phase separation into a light, predominantly aqueous liquid phase and a heavy, predominantly organic liquid phase, and the heavy phase then can be returned to the distillation pot until the water content of the original mixture is substantially exhausted. Temperatures at which the condensate can be cooled can range from about -20° C. to about 75° C., more usually about 0°-30° C., employing any convenient pressure such as atmospheric pressure to maintain substantially liquid phase.

Workup

  1. distillationcan be distilled

Sources & evidence

ORD record
ord-192221853d77421abfb1061281b843f9
Source dataset
uspto-grants-1979_05
Patent number
US04156791

Linked notes

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