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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 2-Chloro-4-(5-tosylthiophen-2-yl)pyrimidine

HRID 2267333
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2267333
C([Li])CCC.[S:6]([C:16]1[S:17][CH:18]=[CH:19][CH:20]=1)([C:9]1[CH:15]=[CH:14][C:12]([CH3:13])=[CH:11][CH:10]=1)(=[O:8])=[O:7].[Cl:21][C:22]1[N:27]=[CH:26][CH:25]=[CH:24][N:23]=1.ClC1C(=O)C(C#N)=C(C#N)C(=O)C=1Cl.[OH-].[Na+]>O1CCCC1>[Cl:21][C:22]1[N:27]=[C:26]([C:18]2[S:17][C:16]([S:6]([C:9]3[CH:10]=[CH:11][C:12]([CH3:13])=[CH:14][CH:15]=3)(=[O:7])=[O:8])=[CH:20][CH:19]=2)[CH:25]=[CH:24][N:23]=1
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Komponenten

7

Edukt 5

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 14798Sodium HydroxideHCID 744042-ChloropyrimidineHCID 2555212-TosylthiopheneHCID 178418339Butyllithium

Produkt 1

HCID 602044282-Chloro-4-(5-tosylthiophen-2-yl)pyrimidineAusbeute 49,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

n-Butyllithium in hexanes (0.92 mL, 2.5 M, 2.30 mmol) was added dropwise to a solution of 2-tosylthiophene (0.5 g, 2.09 mmol) in anhydrous tetrahydrofuran (30 mL) at −78° C. The resulting mixture was stirred at −78° C. for 1 h and a solution of 2-chloropyrimidine (0.26 g, 2.30 mmol) in 3 mL of tetrahydrofuran was added slowly. The mixture was stirred at −78° C. for 1 h and then at −40° C. for 2 h. The reaction was quenched with a solution (0.22 mL) of acetic acid and methanol (1:1) at −40° C. and a solution of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (0.57 g, 2.51 mmol) was added. After complete addition the reaction was stirred for 1 h, and then warmed to rt and stirred for an additional 15 h. 20 mL of aqueous sodium hydroxide (2 M) was added and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic layer was washed with brine (80 mL), dried over anhydrous sodium sulfate and filtered. The solvent was evaporated in vacuo and the product was purified by flash chromatography eluting with ethyl acetate/hexane (1:3) to afford the title compound as a white solid (0.36 g, 49%).

Aufarbeitung

  1. stirringThe mixture was stirred at −78° C. for 1 h
  2. waitat −40° C. for 2 h
  3. customThe reaction was quenched with a solution (0.22 mL) of acetic acid and methanol (1:1) at −40° C.
  4. additionAfter complete addition the reaction
  5. stirringwas stirred for 1 h
  6. temperaturewarmed to rt
  7. stirringstirred for an additional 15 h
  8. extractionthe mixture was extracted with ethyl acetate (3×50 mL)
  9. washThe combined organic layer was washed with brine (80 mL)
  10. dry with materialdried over anhydrous sodium sulfate
  11. filtrationfiltered
  12. customThe solvent was evaporated in vacuo
  13. customthe product was purified by flash chromatography
  14. washeluting with ethyl acetate/hexane (1:3)

Quellen und Nachweise

ORD-Eintrag
ord-fa321bbbc6a34b33abfac00e12d9fb54
Quelldatensatz
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07858785B2

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