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Diethylene Glycol Monoethyl Ether → 4-(2-Fluorophenyl)butanoic acid

HRID 1683478
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1683478
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9]CC#N.[OH-:13].[Na+].C(OCCO[CH2:21][CH2:22][OH:23])C>>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9][CH2:21][C:22]([OH:23])=[O:13]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 8146Diethylene Glycol Monoethyl EtherHCID 14798Sodium HydroxideHCID 224495394-(2-Fluorophenyl)butanenitrile

Produkt 1

HCID 154910364-(2-Fluorophenyl)butanoic acid

Versuchsvorschrift

15.4 gm of the compound prepared in (5) above was added to a mixture of 400 ml of 5% aqueous solution of sodium hydroxide and 400 ml of diethylene glycol monoethyl ether. The mixture was heated under reflux for 3.5 hours, cooled to room temperature, and washed with ether. After the addition of concentrated hydrochloric acid to acidify, the water layer was extracted twice with 500 ml of ethyl acetate. The extract was washed with water and saturated brine in this order, and dried over anhydrous sodium sulfate. The solvent was evaporated to obtain 15.9 gm of the title compound.

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 3.5 hours
  3. washwashed with ether
  4. additionAfter the addition of concentrated hydrochloric acid
  5. extractionthe water layer was extracted twice with 500 ml of ethyl acetate
  6. washThe extract was washed with water and saturated brine in this order
  7. dry with materialdried over anhydrous sodium sulfate
  8. customThe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-129265f3bda84bedb8fbdc576c83708c
Quelldatensatz
uspto-grants-1997_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05637770

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