تفاعل #53378

ord-25ced7eb4bce4b60b9dcf3c7dc51c11f

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe solvent was removed under reduced pressure
  2. 2
    workup.ADDITIONEthyl acetate (150 mL) was added to the residue
  3. 3
    غسيلthe mixture was washed with 2N HCl, brine and water
  4. 4
    أخرىThe organic fraction was isolated
  5. 5
    تجفيفdried with sodium sulfate
  6. 6
    أخرىthe solvent was removed under reduced pressure

الإجراء التجريبي

4-Iodoanisol (10 g, 42 mmol), palladium (II) chloride (0.2 g, 1.1 mmol) and triphenylphosphine (0.6 g, 2.2 mmol) were dissolved in diethylamine (100 mL) then cupper(I) iodide (0.5 g, 2.2 mmol) and 4-pentyn-1-ol (5 mL, 53 mmol) were added. The reaction mixture was stirred overnight at room temperature, then the solvent was removed under reduced pressure. Ethyl acetate (150 mL) was added to the residue and the mixture was washed with 2N HCl, brine and water. The organic fraction was isolated, dried with sodium sulfate and the solvent was removed under reduced pressure. The product 16 (7.1 g. 87%) was isolated by flash chromatography (silica gel, 1:2 ethyl acetate/hexanes) as an oily yellow solid. 1H NMR (300 MHz, CDCl3) δ1.88 (m, 2H), 2.53 (m, 2H), 3.72 (s, 3H), 3.74 (m, 2H), 6.83 (d, 2H), 7.45 (d, 2H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06858614B2uspto-grants-2005_02