2,3,3,3-Tetrafluoro-2-(1,1,2,2,3,3,3-heptafluoropropoxy)propanoyl fluoride → Potassium 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)propanoate

HRID 3947

Reaktionsgleichung

Reaktionsgleichung von HRID 3947
[F:1][C:2]([C:17]([F:20])([F:19])[F:18])([O:6][C:7]([F:16])([F:15])[C:8]([F:14])([F:13])[C:9]([F:12])([F:11])[F:10])[C:3](F)=[O:4].C[Si](C)(C)[O-:23].[K+:26]>CCOCC>[F:1][C:2]([C:17]([F:18])([F:19])[F:20])([O:6][C:7]([F:15])([F:16])[C:8]([F:13])([F:14])[C:9]([F:12])([F:10])[F:11])[C:3]([O-:4])=[O:23].[K+:26]

Komponenten

4

Edukt 2

HCID 1027402,3,3,3-Tetrafluoro-2-(1,1,2,2,3,3,3-heptafluoropropoxy)propanoyl fluorideHCID 23668039Potassium trimethylsilanolate

Produkt 1

HCID 4256185Potassium 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)propanoateAusbeute 72 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

The procedure of Example 1 was followed using perfluoro-2-methyl-3-oxahexanoyl fluoride (16.6 g, 50 mmol), potassium trimethylsilanolate (6.41 g, 50 mmol), and dry ether (300 mL). Potassium perfluoro-2-methyl-3-oxahexanoate (12.3 g initially and 0.9 g by concentrating the filtrate under vacuum; total: 13.2 g, 72% yield) was isolated as a white solid: 19F NMR (D2O) δ -81.0 ##STR12##

Aufarbeitung

  1. concentrationPotassium perfluoro-2-methyl-3-oxahexanoate (12.3 g initially and 0.9 g by concentrating the filtrate under vacuum
  2. customtotal: 13.2 g, 72% yield) was isolated as a white solid

Quellen und Nachweise

ORD-Eintrag
ord-e19db06fc1b6482fb435307594c07f67
Quelldatensatz
uspto-grants-1988_02
Patentnummer
US04723016

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