2,5-Dibromopyridine → 5-Bromo-2-(4-fluorophenyl)pyridine

HRID 1796049Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1796049
Br[C:2]1[CH:7]=[CH:6][C:5]([Br:8])=[CH:4][N:3]=1.[F:9][C:10]1[CH:15]=[CH:14][C:13](B(O)O)=[CH:12][CH:11]=1>COCCOC.C(=O)([O-])[O-].[Na+].[Na+].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>[Br:8][C:5]1[CH:6]=[CH:7][C:2]([C:13]2[CH:14]=[CH:15][C:10]([F:9])=[CH:11][CH:12]=2)=[N:3][CH:4]=1

Komponenten

6

Edukt 2

HCID 693532,5-DibromopyridineHCID 2856454-Fluorophenylboronic acid

Produkt 1

HCID 221807795-Bromo-2-(4-fluorophenyl)pyridineAusbeute 88,4 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 178418397HCID 178418397, VerbindungKatalysatorHCID 80711,2-DimethoxyethaneLösungsmittelHCID 10340Sodium CarbonateLösungsmittel

Versuchsvorschrift

To a degassed mixture of 2,5-dibromopyridine (500 mg, 2.11 mmol) and 4-fluorobenzeneboronic acid (444 mg, 3.17 mmol) in ethylene glycol dimethyl ether (4.2 ml) and 2M aqueous sodium carbonate (2.1 ml) was added tetrakis(triphenylphosphine)palladium(0) (98 mg, 0.08 mmol). This mixture was heated at reflux for 14 h. After cooling the crude reaction was partitioned between water and dichloromethane. The organics were dried over anhydrous magnesium sulfate, filtered and adsorbed onto silica. Purification by chromatography on silica gel, eluting with a mixture of 4% diethyl ether in isohexane, gave 5-bromo-2-(4-fluorophenyl)pyridine (470 mg) as a white solid: δH (360 MHz, CDCl3) 7.30 (1H, d, J 7), 7.12-7.19 (2H, m), 7.57 (1H, d, J 8), 7.86 (1H, dd, J 2 and 8), 7.92-7.98 (2H, m), 8.72 (1H, d, J 2), m/z (ES+) 251, 252, 253, 254 (M++H).

Aufarbeitung

  1. temperatureThis mixture was heated
  2. temperatureat reflux for 14 h
  3. temperatureAfter cooling the crude
  4. customreaction
  5. customwas partitioned between water and dichloromethane
  6. dry with materialThe organics were dried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. customPurification by chromatography on silica gel
  9. washeluting with a mixture of 4% diethyl ether in isohexane

Quellen und Nachweise

ORD-Eintrag
ord-7cf2865dc7b64592a7c48a2c8e137ec7
Quelldatensatz
uspto-grants-2006_04
Patentnummer
US07030128B2

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