Phosphoric acid, disodium salt, dodecahydrate → 2-(3,5-Difluoro-4'-propylbiphenyl-4-yl)-5-propylthiophene

HRID 1399410Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1399410
Br[C:2]1[S:3][C:4]([CH2:7][CH2:8][CH3:9])=[CH:5][CH:6]=1.[CH2:10]([C:13]1[CH:18]=[CH:17][C:16]([C:19]2[CH:24]=[C:23]([F:25])[C:22](B(O)O)=[C:21]([F:29])[CH:20]=2)=[CH:15][CH:14]=1)[CH2:11][CH3:12].P([O-])(O)(O)=O.[Na+].O.O.O.O.O.O.O.O.O.O.O.O.P([O-])([O-])(O)=O.[Na+].[Na+]>C1(C)C=CC=CC=1.O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[F:25][C:23]1[CH:24]=[C:19]([C:16]2[CH:17]=[CH:18][C:13]([CH2:10][CH2:11][CH3:12])=[CH:14][CH:15]=2)[CH:20]=[C:21]([F:29])[C:22]=1[C:2]1[S:3][C:4]([CH2:7][CH2:8][CH3:9])=[CH:5][CH:6]=1

Komponenten

8

Edukt 4

HCID 61456Phosphoric acid, disodium salt, dodecahydrateHCID 218019042-Bromo-5-propylthiopheneHCID 23672064Monosodium phosphateHCID 580284314'-Propyl-3,5-difluoro-4-biphenylboronic acid

Produkt 1

HCID 580284282-(3,5-Difluoro-4'-propylbiphenyl-4-yl)-5-propylthiophene

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 178418397HCID 178418397, VerbindungKatalysatorHCID 962WaterLösungsmittelHCID 1140TolueneLösungsmittel

Versuchsvorschrift

5.0 g (24.4 mmol) of 2-bromo-5-propylthiophene, 7.40 g (26.8 mmol) of 4′-propyl-3,5-difluoro-4-biphenylboronic acid and 2.82 g (2.44 mmol) of tetrakis(triphenylphosphine)palladium(0) are initially introduced in 160 ml of toluene. A solution of 5.85 g (48.8 mmol) of sodium dihydrogenphosphate and 13.8 g (97.5 mmol) of disodium hydrogenphosphate dodecahydrate in 50 ml of water is added, and the mixture is heated under reflux for 19 h. After cooling, the organic phase is separated off, and the aqueous phase is extracted a number of times with toluene. The combined organic phases are washed with water and sat. sodium chloride solution. The solution is dried using sodium sulfate and evaporated to dryness. The residue is purified by column chromatography (SiO2, n-heptane). Further purification is carried out by recrystallisation from ethanol and n-heptane, giving 2-(3,5-difluoro-4′-propylbiphenyl-4-yl)-5-propylthiophene (PUS-3-3) as a colourless solid (m.p. 64° C.).

Aufarbeitung

  1. temperaturethe mixture is heated
  2. temperatureunder reflux for 19 h
  3. temperatureAfter cooling
  4. customthe organic phase is separated off
  5. extractionthe aqueous phase is extracted a number of times with toluene
  6. washThe combined organic phases are washed with water and sat. sodium chloride solution
  7. customThe solution is dried
  8. customevaporated to dryness
  9. customThe residue is purified by column chromatography (SiO2, n-heptane)
  10. customFurther purification
  11. customis carried out by recrystallisation from ethanol and n-heptane

Quellen und Nachweise

ORD-Eintrag
ord-6abfc42a60b04f8f9a31f176251b538d
Quelldatensatz
uspto-grants-2014_12
Patentnummer
US08906261B2

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