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Lithium hydroxide, monohydrate → 4,4,4-Trifluorobutanoic acid

HRID 1198300
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1198300
O.[OH-].[Li+].[F:4][C:5]([F:14])([F:13])[CH2:6][CH2:7][C:8]([O:10]CC)=[O:9]>O.CO.O1CCCC1>[F:4][C:5]([F:14])([F:13])[CH2:6][CH2:7][C:8]([OH:10])=[O:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 2

HCID 168937Lithium hydroxide, monohydrateHCID 2733273Ethyl 4,4,4-Trifluorobutyrate

Produkt 1

HCID 27770854,4,4-Trifluorobutanoic acidAusbeute 95,3 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittel
HCID 8028
Tetrahydrofuran
Lösungsmittel

Versuchsvorschrift

A solution of lithium hydroxide monohydrate (324 g) in water (1.8 l) was added to a stirred solution of ethyl 4,4,4-trifluorobutyrate (436 g) in methanol (2.0 l) and dry tetrahydrofuran (2.0 l) and the suspension was stirred overnight. After the suspension was partially evaporated, the residue was diluted with water and washed with diethyl ether. The aqueous layer was acidified with 6M hydrochloric acid and extracted with diethyl ether. The combined extracts were washed (brine), dried (MgSO4), and filtered. The filtrate was evaporated and the residue distilled (b.p. 165°-168° C.) to give 4,4,4-trifluorobutyric acid (347 g, 95%); m.p. 27°-30° C.; partial NMR; (300 MHz, CDCl3): 2.33-2.57 (m, 2H, CF3CH2), 2.66 (t, CH2CO2H).

Aufarbeitung

  1. customAfter the suspension was partially evaporated
  2. additionthe residue was diluted with water
  3. washwashed with diethyl ether
  4. extractionextracted with diethyl ether
  5. washThe combined extracts were washed (brine)
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customThe filtrate was evaporated
  9. distillationthe residue distilled (b.p. 165°-168° C.)

Quellen und Nachweise

ORD-Eintrag
ord-1574d2047ca541b4aa9df6dffc535f46
Quelldatensatz
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05280125

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