تفاعل #55871

ord-c49a5a66e8e9498c8e752722cf12a997

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITAfter 10 min.
  2. 2
    درجة الحرارةthe mixture was gradually heated up
  3. 3
    درجة الحرارةwas heated
  4. 4
    درجة الحرارةunder reflux for 2 hr
  5. 5
    أخرىafter removal of most of the solvent
  6. 6
    workup.DISTILLATIONby distillation under a reduced pressure, diethylether
  7. 7
    workup.ADDITIONwas added
  8. 8
    أخرىThe ether layer was separated
  9. 9
    غسيلwashed with water
  10. 10
    تجفيفdried with anhydrous magnesium sulfate
  11. 11
    ترشيحAfter filtration
  12. 12
    تركيزthe filtrate was concentrated under a reduced pressure
  13. 13
    أخرىthe residue was purified by silica gel column chromatography (ethyl acetate: n-hexane=1:4)

الإجراء التجريبي

Under an argon atmosphere, potassium hydroxide (1.12 g, 20 mmol) was dissolved in methanol (10 ml). Thiophenol (0.6 g, 5.45 mmol) was added to this solution with stirring and under water cooling. After 10 min., a solution of α-trichloromethyl-2-thiophenemethanol (1.16 g, 5 mmol) in methanol (3 ml) was added. After 10 min., the mixture was gradually heated up and was heated under reflux for 2 hr. with vigorous stirring. After cooling to room temperature and after removal of most of the solvent by distillation under a reduced pressure, diethylether was added and the mixture was decomposed with dilute hydrochloric acid. The ether layer was separated, washed with water, and dried with anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under a reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate: n-hexane=1:4) to give 940 mg of α-phenylthio-2-thiopheneacetic acid as a viscous oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04221915uspto-grants-1980_09