تفاعل #93214

ord-cd4af154a0b14d2aa520efa5a6a262e6

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
-5°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةmaintained under a nitrogen atmosphere
  2. 2
    درجة الحرارةso as to maintain the reaction temperature at -5° C. to 0° C
  3. 3
    درجة الحرارةthe reactor was maintained at -2° C. to 5° C. for an additional 50 minutes (3000 s)
  4. 4
    استخلاصAfter 5 minutes (300 s) the water and product mixture was extracted with three 500 milliliter portions of methylene chloride
  5. 5
    استخلاصThe combined methylene chloride extract
  6. 6
    غسيلwas washed with 500 milliliters of 5 percent aqueous hydrochloric acid
  7. 7
    غسيلby washing with 800 milliliters of deionized water
  8. 8
    تجفيفthen drying over anhydrous sodium sulfate
  9. 9
    ترشيحThe dry methylene chloride solution was filtered
  10. 10
    أخرىsolvent removed by rotary evaporation under vacuum
  11. 11
    أخرىBisphenol A dicyanate (360.7 grams) was recovered in 86.4 percent yield as a white crystalline solid

الإجراء التجريبي

A 342.45 gram (1.5 moles) portion of bisphenol A, 333.68 grams (3.15 moles) of cyanogen bromide and 1000 milliliters of acetone were added to a reactor and maintained under a nitrogen atmosphere with stirring. The stirred solution was cooled to -5° C. then 305.09 grams (3.015 moles) of triethylamine was added to the reactor over a twenty-five minute (1500 s) period and so as to maintain the reaction temperature at -5° C. to 0° C. After completion of the triethylamine addition, the reactor was maintained at -2° C. to 5° C. for an additional 50 minutes (3000 s), followed by addition of the reactor contents to 1 gallon (3.79 l) of chilled deionized water. After 5 minutes (300 s) the water and product mixture was extracted with three 500 milliliter portions of methylene chloride. The combined methylene chloride extract was washed with 500 milliliters of 5 percent aqueous hydrochloric acid followed by washing with 800 milliliters of deionized water then drying over anhydrous sodium sulfate. The dry methylene chloride solution was filtered and solvent removed by rotary evaporation under vacuum. Bisphenol A dicyanate (360.7 grams) was recovered in 86.4 percent yield as a white crystalline solid. Infrared spectrophotometric analysis of a film sample of the product confirmed the product structure (disappearance of phenolic hydroxyl absorbance, appearance of --O--C≡N absorbance).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04611022uspto-grants-1986_09