反应 #312575

ord-ba0ce24846e3467bbeefbf4f3f25d544

反应方程式

COc1ccc(C(=O)c2ccc(F)cc2)cc1
4-Fluoro-4′-methoxy-benzophenone
COc1ccc(C(=O)c2ccc(F)cc2)cc1
4-fluoro-4′-methoxy-benzophenone
C#C
acetylene
[C-]#[C-].[Na+].[Na+]
Sodium acetylide
C#CC(O)(c1ccc(F)cc1)c1ccc(OC)cc1
1-(4-fluorophenyl)-1-(4-methoxyphenyl)-2-propyn-1-ol

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他separated
  2. 2
    萃取the aqueous layer was extracted with three portions of diethyl ether (200 mL)
  3. 3
    洗涤washed with saturated aqueous NH4Cl (200 mL), saturated aqueous NaCl (200 mL), and saturated aqueous sodium bicarbonate (200 mL)
  4. 4
    干燥The organic layer was dried over anhydrous sodium sulfate
  5. 5
    其他evaporated to an amber colored oil

实验过程

4-Fluoro-4′-methoxy-benzophenone from Step 1 (126.7 grams) and acetylene saturated N,N-dimethylformamide (380 mL) were combined in a reaction flask. Sodium acetylide solution (9 weight % in toluene, 343 grams) was added to the reaction mixture dropwise over 45 minutes. The reaction mixture was stirred at room temperature for 1 hour and then poured into ice water (600 mL). The layers were phase separated and the aqueous layer was extracted with three portions of diethyl ether (200 mL). The organic layers were combined and washed with saturated aqueous NH4Cl (200 mL), saturated aqueous NaCl (200 mL), and saturated aqueous sodium bicarbonate (200 mL). The organic layer was dried over anhydrous sodium sulfate and evaporated to an amber colored oil yielding 136.6 grams of 1-(4-fluorophenyl)-1-(4-methoxyphenyl)-2-propyn-1-ol. This material was not purified further but was used directly in the next step.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07556751B2uspto-grants-2009_07