تفاعل #81699

ord-00562ed35dad4109b64de54373779ed5

المتفاعلات

الكواشف

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المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىInto a 500 cc four-necked equipped with a stirrer, a reflux condenser, a dropping funnel
  2. 2
    درجة الحرارةThe reactor was heated
  3. 3
    أخرىto 60° C
  4. 4
    workup.ADDITIONAfter completion of the dropwise addition
  5. 5
    درجة الحرارةheating
  6. 6
    درجة الحرارةrefluxing
  7. 7
    workup.WAITwere continued for 10 hours
  8. 8
    workup.DISSOLUTIONto dissolve
  9. 9
    أخرىprecipitated potassium iodide
  10. 10
    أخرىThe crude reaction solution
  11. 11
    أخرىwas separated into two layers
  12. 12
    غسيلthe fluorocarbon layer (lower layer) was further washed with 300 g of water

الإجراء التجريبي

Into a 500 cc four-necked equipped with a stirrer, a reflux condenser, a dropping funnel and a thermometer, 200 cc of methanol and 32.4 g (0.6 mol) of sodium methoxide were charged. The reactor was heated to bring the internal temperature to 60° C. Then, 273 g of (0.5 mol) of C8F17I was dropwise added thereto over a period of one hour. After completion of the dropwise addition, heating and refluxing were continued for 10 hours. The conversion at that time was 99.8%. The reactor was cooled to room temperature. Then, 300 g of water was added to dissolve precipitated potassium iodide. The crude reaction solution was separated into two layers, and the fluorocarbon layer (lower layer) was further washed with 300 g of water to obtain 201 g of C8F17H having a purity of 99.4%. In the reactor, no formation of tar was observed.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05618986uspto-grants-1997_04