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2,5-Difluoroaniline → N-(2,5-difluorophenyl)[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-methyl]amine

HRID 48074
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 48074
[F:1][C:2]1[CH:8]=[CH:7][C:6]([F:9])=[CH:5][C:3]=1[NH2:4].[F:10][C:11]([F:24])([O:15][C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][CH:23]=1)[CH:19]=O)[CH:12]([F:14])[F:13]>C1CCCCC1>[F:1][C:2]1[CH:8]=[CH:7][C:6]([F:9])=[CH:5][C:3]=1[NH:4][CH2:19][C:18]1[CH:21]=[CH:22][CH:23]=[C:16]([O:15][C:11]([F:10])([F:24])[CH:12]([F:13])[F:14])[CH:17]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 677752,5-DifluoroanilineHCID 118803Benzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-

Produkt 1

HCID 11002165N-(2,5-difluorophenyl)[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-methyl]amineAusbeute 86 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8078CyclohexaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Ex-661A) A mixture of 2,5-difluoroaniline (2.58 g, 20 mmol) and 3-(1,1,2,2-tetrafluoroethoxy)benzaldehyde (4.44 g, 20 mmol) in cyclohexane (50 mL) was heated under reflux for 5 h using a Dean-Stark trap to remove water. The solvent was removed in vacuo, and the residue was dissolved in methanol (30 mL). The solution was stirred and cooled to 0° C., then sodium borohydride was added (1.32 g, 35 mmol). The mixture was allowed to warm to room temperature and stirred for 2 h, then acidified with 1 N HCl. After neutralizing to pH 7.5 with 2.5 N sodium hydroxide, the mixture was extracted with diethyl ether (3×20 mL). The organic layer was washed with brine and water, then dried over anhydrous MgSO4, and evaporated to give 5.7 g (86%) of the desired N-(2,5-difluorophenyl)[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-methyl]amine product as a brown oil, which was greater than 90% pure by reverse phase HPLC analysis. MS m/z=336 [M+].

Aufarbeitung

  1. temperaturewas heated
  2. temperatureunder reflux for 5 h
  3. customto remove water
  4. customThe solvent was removed in vacuo
  5. dissolutionthe residue was dissolved in methanol (30 mL)
  6. additionsodium borohydride was added (1.32 g, 35 mmol)
  7. temperatureto warm to room temperature
  8. stirringstirred for 2 h
  9. extractionthe mixture was extracted with diethyl ether (3×20 mL)
  10. washThe organic layer was washed with brine and water
  11. dry with materialdried over anhydrous MgSO4
  12. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-fc685d8093c1439dae30b6bcfe396b5b
Quelldatensatz
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06699898B2

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