Potassium Fluoride → 3,4',4''-Tri(diethoxyphosphoryl)-[2,2';5',2'']-terthiophene

HRID 1662887Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1662887
[CH2:1]([O:3][P:4]([C:9]1[CH:10]=[C:11]([C:14]2[S:15][C:16](I)=[CH:17][C:18]=2[P:19]([O:24][CH2:25][CH3:26])([O:21][CH2:22][CH3:23])=[O:20])[S:12][CH:13]=1)([O:6][CH2:7][CH3:8])=[O:5])[CH3:2].C([Sn](CCCC)(CCCC)[C:33]1[S:34][CH:35]=[CH:36][C:37]=1[P:38]([O:43][CH2:44][CH3:45])([O:40][CH2:41][CH3:42])=[O:39])CCC.[Cu]C#N.[F-].[K+]>C1(C)C=CC=CC=1>[CH2:22]([O:21][P:19]([C:18]1[CH:17]=[CH:16][S:15][C:14]=1[C:11]1[S:12][C:13]([C:35]2[S:34][CH:33]=[C:37]([P:38]([O:40][CH2:41][CH3:42])([O:43][CH2:44][CH3:45])=[O:39])[CH:36]=2)=[C:9]([P:4]([O:6][CH2:7][CH3:8])([O:3][CH2:1][CH3:2])=[O:5])[CH:10]=1)([O:24][CH2:25][CH3:26])=[O:20])[CH3:23]

Komponenten

6

Edukt 4

HCID 522689Potassium FluorideHCID 59155833HCID 59155833, VerbindungHCID 591558664,3'-Bis(diethoxyphosphoryl)-5'-iodo-[2,2']-bithiopheneHCID 178418546HCID 178418546, Verbindung

Produkt 1

HCID 591558983,4',4''-Tri(diethoxyphosphoryl)-[2,2';5',2'']-terthiopheneAusbeute 70 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

At room temperature, 0.1129 g (0.2 mmols) of 4,3′-bis(diethoxyphosphoryl)-5′-iodo-[2,2′]-bithiophene and 0.0092 g (0.008 mmols) of commercially available tetrakistriphenylphosphine palladium were dissolved in 2 ml of toluene, to which 0.1018 g (0.2 mmols) of 2-(tributylstannyl)-3-(diethoxyphosphoryl)thiophene and 0.0036 g (0.04 mmols) of commercially available copper(I) cyanide were added at room temperature. Thereafter, the reaction mixture was heated and stirred under reflux for 2.5 hours. After the reaction, the reaction mixture was cooled down to room temperature, to which a potassium fluoride aqueous solution added, followed by stirring for 1 hour. The resulting solid was removed by celite filtration and the filtrate was extracted with ethyl acetate. The organic phase was washed with a saturated saline solution and dried over anhydrous sodium sulfate. The solvent was removed by distilling off under reduced pressure, and the resulting crude product was purified with a PTLC plate (developed with ethyl acetate:hexane=1:2 and ethyl acetate:hexane=1:1) to obtain the specified substance in the form of a yellow oil at a yield of 0.0919 g (yield: 70%).

Aufarbeitung

  1. additionwere added at room temperature
  2. temperatureThereafter, the reaction mixture was heated
  3. temperatureunder reflux for 2.5 hours
  4. customAfter the reaction
  5. additionadded
  6. stirringby stirring for 1 hour
  7. customThe resulting solid was removed by celite filtration
  8. extractionthe filtrate was extracted with ethyl acetate
  9. washThe organic phase was washed with a saturated saline solution
  10. dry with materialdried over anhydrous sodium sulfate
  11. customThe solvent was removed
  12. distillationby distilling off under reduced pressure
  13. customthe resulting crude product was purified with a PTLC plate (developed with ethyl acetate:hexane=1:2 and ethyl acetate:hexane=1:1)
  14. customto obtain the specified substance in the form of a yellow oil at a yield of 0.0919 g (yield: 70%)

Quellen und Nachweise

ORD-Eintrag
ord-ce0d56b2d4ad4e47901722c560466730
Quelldatensatz
uspto-grants-2011_10
Patentnummer
US08030438B2

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