反应 #1253206

ord-6bb04464ee3a436dbb23605c0d87f182

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他some precipitate formed
  2. 2
    其他The reaction was quenched carefully with 1 N HCl
  3. 3
    萃取extracted with CH2Cl2
  4. 4
    干燥the combined organic phase was dried over MgSO4
  5. 5
    其他The crude product was obtained as off-white solid
  6. 6
    其他was recrystallized from acetone

实验过程

Compound 7 (19.2 g, 0.059 mol) was dissolved in 100 mL of dry CH2Cl2, and aluminum chloride (16.6 g, 0.12 mol) was added. The reaction turned orange and some precipitate formed. The reaction was cooled to 0° C., and phenyldecane (45.3 g, 0.21 mol) in 50 mL of dry CH2Cl2 was added through an additional funnel. The reaction was stirred at room temperature under nitrogen overnight. The reaction was quenched carefully with 1 N HCl, extracted with CH2Cl2, and the combined organic phase was dried over MgSO4. The crude product was obtained as off-white solid and was recrystallized from acetone to give 31.8 g of pure product as white crystals at 74% yield. 1H NMR (CDCl3) δ (ppm): 0.88 (t, J=6.7 Hz, 6H), 1.26-1.32 (m, 28H), 1.62-1.67 (m, 4H), 2.69 (t, J=7.6 Hz, 4H), 7.32 (d, J=7.9 Hz, 4H), 7.58 (s, 2H), 7.76 (d, J=7.9 Hz, 4H). Mp 128-129° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06613457B2uspto-grants-2003_09