反应详情

温度

-5 °C

A 201.26 gram (1.50 mole) portion of p-isopropenyl phenol, 166.84 grams (1.575 mole) of cyanogen bromide and 900 milliliters of acetone were added to a reactor and maintained under a nitrogen atmosphere with stirring. The p-isopropenyl phenol used herein was of in excess of 99 percent purity. The stirred solution was cooled to -5° C. then 151.79 grams (1.50 mole) of triethylamine was added to the reactor over a twenty minute (1200 s) period and so as to maintain the reaction temperature at -5° to 0° C. After completion of the triethylamine addition, the reactor was maintained at -3° to 5° C. for an additional thirty-two minutes (1820 s), followed by addition of the reactor contents to 1 gallon of chilled deionized water. After five minutes (300 s) the water and product mixture was multiply extracted with three 400 milliliter volumes 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 extract was filtered and solvent removed by rotary evaporation under vacuum. p-Isopropenylphenyl cyanate (207.24 grams) was recovered in 86.8 percent yield as a transparent, light amber colored liquid. Infrared spectrophotometric analysis of a film sample of the product confirmed the product structure (disappearance of phenolic hydroxyl group, appearance of --C≡N group). Gas chromatographic-mass spectroscopic analysis of the produuct confirmed the structure of p-isopropenylphenyl cyanate (parent ion m/e=159) with essentially no other compounds being present.

1. temperaturemaintained under a nitrogen atmosphere
2. temperatureso as to maintain the reaction temperature at -5° to 0° C
3. temperaturethe reactor was maintained at -3° to 5° C. for an additional thirty-two minutes (1820 s)
4. extractionAfter five minutes (300 s) the water and product mixture was multiply extracted with three 400 milliliter volumes of methylene chloride
5. extractionThe combined methylene chloride extract
6. washwas washed with 500 milliliters of 5 percent aqueous hydrochloric acid
7. washby washing with 800 milliliters of deionized water
8. dry with materialthen drying over anhydrous sodium sulfate
9. extractionThe dry methylene chloride extract
10. filtrationwas filtered
11. customsolvent removed by rotary evaporation under vacuum
12. customp-Isopropenylphenyl cyanate (207.24 grams) was recovered in 86.8 percent yield as a transparent, light amber colored liquid