تفاعل #10306

ord-c1acfb3adf39446d8b5e3103b040d2f4

معادلة التفاعل

Cc1cc(F)ccc1Br
2-bromo-5-fluorotoluene
C=COCCCC
butyl vinyl ether
c1ccc(P(CCCP(c2ccccc2)c2ccccc2)c2ccccc2)cc1
1,3-bis(diphenylphosphino)propane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(=O)c1ccc(F)cc1C
title compound
المردود 49.0%
CC(=O)c1ccc(F)cc1C
1-(4-Fluoro-2-methylphenyl)ethanone
المردود 49.0%

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe cooled reaction mixture
  2. 2
    workup.ADDITIONadded
  3. 3
    أخرىto obtain
  4. 4
    أخرىan easier separation of the 2 layers
  5. 5
    غسيلThe organic layer was washed with brine
  6. 6
    تجفيفdried (MgSO4)
  7. 7
    تركيزconcentrated
  8. 8
    أخرىThe residue was purified on a plug of silica eluting with 3% EtOAc/isohexane

الإجراء التجريبي

To a solution of 2-bromo-5-fluorotoluene (5 g, 26.5 mmol) in DMF (65 ml) and water (15 ml) was added butyl vinyl ether (6.6 g, 65.9 mmol), palladium acetate (0.18 g, 0.8 mmol), 1,3-bis(diphenylphosphino)propane (0.72 g, 1.75 mmol) and potassium carbonate (4.4 g, 31.8 mmol). The reaction was heated at 80° C. for 48 h under nitrogen. The cooled reaction mixture was diluted with EtOAc (˜250 ml) and concentrated HCl added and shaken. Further EtOAc and water were added to obtain an easier separation of the 2 layers. The organic layer was washed with brine, dried (MgSO4), and concentrated. The residue was purified on a plug of silica eluting with 3% EtOAc/isohexane to give the title compound as an oil (1.95 g, 49%). 1H NMR (400 MHz, d6-DMSO) δ 2.45 (3H, s), 2.54 (3H, s), 7.13–7.17 (2H, m), 7.89–7.93 (1H, m).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07094777B2uspto-grants-2006_08