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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745843Generated: November 2, 2026

Acetone → HCID 178439265, compound

https://huagongshe.com/reaction/745843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBisphenol AHCID 6623—
ReactantTriethylamineHCID 8471—
ReactantCyanogen BromideHCID 10476—
SolventWaterHCID 962—
ProductHCID 178439265HCID 17843926588.7%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A 342.5 gram portion of 4,4'-isopropylidenediphenol (1.50 moles), 333.68 grams of cyanogen bromide (3.15 moles) 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 of triethylamine (3.015 moles) was added to the reactor over a twenty-four minute (1440 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 0° to 7° C. for an additional forty-five minutes (2700 s), followed by addition of the reactor contents to 1 gallon of chilled deionized water. After twenty minutes (1200 s) the water and product mixture was filtered and the recovered crude crystalline product was dissolved in 1000 milliliters of methylene chloride. The methylene chloride solution was washed with 500 milliliters of 5 percent aqueous hydrochloric acid followed by washing with 500 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 (370.3 grams) was recovered in 88.7 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 numberUS04600760
Source datasetuspto-grants-1986_07
ORD IDord-223360942ae542a7beb4be9f6d20add8
Source noteuspto-grants-1986_07