تفاعل #169929

ord-e967a84eaca949648371400592c1fba9

المتفاعلات

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىPyridine and dichloromethane was evaporated in vacuo
  2. 2
    workup.ADDITIONWater (600 mL) was added
  3. 3
    استخلاصThe reaction mixture was extracted with ethyl acetate (500 mL×3)
  4. 4
    تجفيفthe organic phase was dried over anhydrous sodium sulfate
  5. 5
    ترشيحfiltrated
  6. 6
    تركيزconcentrated
  7. 7
    أخرىpurified by column chromatography (PE:EA=60:1)

الإجراء التجريبي

To a stirred suspension of 3-bromophenol (50 g, 0.29 mol) in pyridine (200 mL) and dichloromethane (100 mL) was added dropwise acetyl chloride (25 mL, 0.35 mol) at 0° C. and the mixture was stirred 18 h at room temperature. LC-MS showed that the reaction was complete. Pyridine and dichloromethane was evaporated in vacuo. Water (600 mL) was added and acidified with hydrochloric acid at pH 2. The reaction mixture was extracted with ethyl acetate (500 mL×3) and the organic phase was dried over anhydrous sodium sulfate, filtrated, concentrated and purified by column chromatography (PE:EA=60:1) to afford compound E-1 as a colorless liquid (46 g, 74%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08846736B2uspto-grants-2014_09