反応 #155400

ord-968a86666c514b66ad2f8f26e08fb3e7

反応方程式

O
water
C=CCCCBr
5-bromo-pentene
O=C([O-])[O-].[K+].[K+]
K2CO3
O=C1NC(=O)c2ccccc21.[K]
potassium phthalimide
C=CCCCN1C(=O)c2ccccc2C1=O
2-(pent-4-enyl)-isoindoline-1,3-dione
収率 87.9%

溶媒

反応条件

温度
100°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction mixture was cooled to room temperature
  2. 2
    抽出The aqueous layer was then extracted with ethyl acetate (2×50 mL)
  3. 3
    洗浄the combined organic layers were washed with 5% aq. NaHCO3 (2×20 mL), brine (30 mL)
  4. 4
    乾燥dried over Na2SO4
  5. 5
    ろ過Filtration and solvent evaporation
  6. 6
    その他gave an oil, which
  7. 7
    その他was purified by flash chromatography (silica gel/hexanes:ethyl acetate 0-35%)

実験手順

To a stirring solution of 5-bromo-pentene (6.0 g, 0.040 mol) in DMF (30 mL) was added K2CO3 (4.7 g, 0.034 mol) and potassium phthalimide (6.21 g, 0.033 mmol) and the reaction mixture was heated at 100° C. for 1 hr. The reaction mixture was cooled to room temperature, and water (50 mL) was added. The aqueous layer was then extracted with ethyl acetate (2×50 mL), and the combined organic layers were washed with 5% aq. NaHCO3 (2×20 mL), brine (30 mL) and dried over Na2SO4. Filtration and solvent evaporation gave an oil, which was purified by flash chromatography (silica gel/hexanes:ethyl acetate 0-35%) to yield the desired 2-(pent-4-enyl)-isoindoline-1,3-dione as a solid (6.36 g, 0.029 mmol, 72.5% yield): MS m/e [M+H]+ calcd 216.1. found 216.1; NMR (250 MHz, DMSO-d6) δ 7.79-7.95 (m, 4H), 5.70-5.91 (m, 1H), 4.90-5.11 (m, 2H), 3.58 (t, 2H), 1.98-2.10 (m, 2H), 1.59-1.78 (m, 2H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08822424B2uspto-grants-2014_09