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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637738Generated: November 1, 2026

Acetone → HCID 178439265, compound

https://huagongshe.com/reaction/637738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBisphenol AHCID 6623—
ReactantTriethylamineHCID 8471—
ReactantCyanogen BromideHCID 10476—
SolventWaterHCID 962—
ProductHCID 178439265HCID 17843926594.3%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A 228.3 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 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 1000 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 (393.8 grams) was recovered in 94.3 percent yield as a white crystalline solid. Infrared spectrophotometric analysis of a film sample of the product confirmed the product structure (disappearance of phenolic hydroxy group, appearance of --C≡N group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04558115
Source datasetuspto-grants-1985_12
ORD IDord-1de2d0be682645789c49d6bee70e00e5
Source noteuspto-grants-1985_12