2-(Allyloxymethyl)-1-fluoro-3-iodobenzene → 8-Fluoro-4-methylene-3,4-dihydro-1H-isochromene

HRID 1363156Notes

Reaction equation

HRID 1363156 reaction equation
[CH2:1]([O:4][CH2:5][C:6]1[C:11](I)=[CH:10][CH:9]=[CH:8][C:7]=1[F:13])[CH:2]=[CH2:3]>CC#N.CCN(CC)CC>[F:13][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]2[C:6]=1[CH2:5][O:4][CH2:1][C:2]2=[CH2:3]

Participants

4

Conditions

Temperature
80 °C

Procedure

2-(Allyloxymethyl)-1-fluoro-3-iodobenzene (1 g) was dissolved in 20 mL of CH3CN and 2.4 mL of Et3N. The reaction solution was vacuum degassed three times, followed by the addition of Pd(OAc)2 (37.6 mg) and PPh3 (89.8 mg). The resulting mixture was heated at 80° C. for 16 hours. The reaction mixture was cooled to room temperature and diluted with Et2O. The organic layer was washed with 1N HCl, 10% aqueous NaHCO3, brine, and then dried over Na2SO4. After filtration, the filtrate was concentrated to dryness to offer a brown oil, which was purified by flash chromatography to offer 200 mg of the title compound.

Workup

  1. customdegassed three times
  2. additionfollowed by the addition of Pd(OAc)2 (37.6 mg) and PPh3 (89.8 mg)
  3. temperatureThe reaction mixture was cooled to room temperature
  4. additiondiluted with Et2O
  5. washThe organic layer was washed with 1N HCl, 10% aqueous NaHCO3, brine
  6. dry with materialdried over Na2SO4
  7. filtrationAfter filtration
  8. concentrationthe filtrate was concentrated to dryness
  9. customwas purified by flash chromatography

Sources & evidence

ORD record
ord-e9261ed7e8694d73b56806cc42dc9730
Source dataset
uspto-grants-2011_02
Patent number
US07884109B2

Reaction notes

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