Cesium carbonate → 2-Methyl-5-vinylpyridine

HRID 2407185Notes

Reaction equation

HRID 2407185 reaction equation
[CH:1]([B-](F)(F)F)=[CH2:2].[K+].Br[C:9]1[CH:10]=[CH:11][C:12]([CH3:15])=[N:13][CH:14]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C([O-])([O-])=O.[Cs+].[Cs+]>O>[CH3:15][C:12]1[CH:11]=[CH:10][C:9]([CH:1]=[CH2:2])=[CH:14][N:13]=1

Participants

6

Conditions

Temperature
77.5 °C

Procedure

Water (10 mL) was added to a mixture of potassium vinyltrifluoroborate (6.35 g, 47.4 mmol, Aldrich), 5-bromo-2-methylpyridine (8.00 g, 46.5 mmol,), triphenylphosphine (0.732 g, 2.79 mmol) and Cs2CO3 (45.5 g, 140 mmol) in a 500 mL round-bottom flask with stir bar. The flask was evacuated and purged with nitrogen (3 cycles), and the mixture was then heated under nitrogen at 75-80° C. for 19 hours, and then cooled to room temperature. The mixture was diluted with water (100 mL) and hexanes (50 mL), and the aqueous layer was drawn off and extracted with ether-hexanes (4:1, 50 mL). The combined organic phases were washed with brine (25 mL), dried over Na2SO4 and distilled at atmospheric pressure to a volume of ca. 10 mL. The residue was distilled under vacuum (90-100° C./20 Torr) to provide the title compound: 1H NMR (400 MHz, methanol-d4) δ ppm 2.51 (s, 3H) 5.35 (d, J=11.1 Hz, 1H) 5.86 (d, J=17.8 Hz, 1H) 6.74 (dd, J=17.8, 11.1 Hz, 1H) 7.27 (d, J=7.9 Hz, 1H) 7.84 (dd, J=8.3, 2.4 Hz, 1H) 8.40 (d, J=2.0 Hz, 1H).

Workup

  1. customThe flask was evacuated
  2. custompurged with nitrogen (3 cycles)
  3. temperaturecooled to room temperature
  4. additionThe mixture was diluted with water (100 mL) and hexanes (50 mL)
  5. extractionextracted with ether-hexanes (4:1, 50 mL)
  6. washThe combined organic phases were washed with brine (25 mL)
  7. dry with materialdried over Na2SO4
  8. distillationdistilled at atmospheric pressure to a volume of ca. 10 mL
  9. distillationThe residue was distilled under vacuum (90-100° C./20 Torr)

Sources & evidence

ORD record
ord-a5164bf1c7144aacbe857e5f09fab0b0
Source dataset
uspto-grants-2014_08
Patent number
US08809532B2

Reaction notes

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