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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638014Generated: October 30, 2026

Acetone → HCID 178439265, compound

https://huagongshe.com/reaction/638014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBisphenol AHCID 6623—
ReactantTriethylamineHCID 8471—
ReactantCyanogen BromideHCID 10476—
SolventWaterHCID 962—
ProductHCID 178439265HCID 17843926586.4%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A 342.45 gram (1.50 moles) portion of 4,4'-isopropylidenediphenol, 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° to 0° C. After completion of the triethylamine addition, the reactor was maintained at -2° 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 group, appearance of --C≡N group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04559399
Source datasetuspto-grants-1985_12
ORD IDord-8df61e1106984b93b26438584a203857
Source noteuspto-grants-1985_12