HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839772Generated: October 30, 2026
Bisphenol A → 1,3-Bis(4-cyanophenyl)propane
https://huagongshe.com/reaction/839772
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bisphenol A | HCID 6623 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyanogen Chloride | HCID 10477 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1,3-Bis(4-cyanophenyl)propane | HCID 70872 | 76% |
Reaction Steps
According to Example 7 of U.S. Pat. No. 3,553,244, 228 parts by weight of 2,2-bis-(4-hydroxyphenyl)-propane are dissolved in 400 parts by weight of acetone and cooled to 0° C. 135 parts by weight of cyanogen chloride are added dropwise at that temperature. 120 parts by weight of triethylamine are then added with external cooling, the temperature being kept below 10° C. On completion of the dropwise addition, the mixture is stirred for 30 minutes, after which the triethylamine hydrochloride which has crystallized out is filtered off. After the acetone has been distilled off, 2,2-bis-(4-cyanatophenyl)-propane is obtained from the filtrate in the form of colorless crystals melting at 77° to 80° C in a quantity of 212 parts by weight (corresponding to a yield of 76%, based on the theoretical amount). The purity amounts to approximately 95% (as determined by IR-spectroscopy).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04097455 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-f106ac6674e3443699de56478f512a3e |
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| Source note | uspto-grants-1978_06 |
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