HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439534Generated: October 26, 2026
Tetrachlorobisphenol A → 2-(3,5-Dichloro-4-hydroxyphenyl)-2-(3,5-dichloro-4-cyanatophenyl)-propane
https://huagongshe.com/reaction/1439534
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrachlorobisphenol A | HCID 6619 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Cyanogen Chloride | HCID 10477 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3,5-Dichloro-4-hydroxyphenyl)-2-(3,5-dichloro-4-cyanatophenyl)-propane | HCID 21395859 | 99.7% |
Reaction Steps
36.6 g (0.1 mol) of 2,2-bis-(3,5-dichloro-4-hydroxyphenyl)-propane are suspended in 500 ml of water and 400 ml of methylene chloride. After cooling to about 0° to 3° C, 20 ml (0.4 mol) of cyanogen chloride are added. A solution of 10.6 g of Na2CO3 in 50 ml of water is added dropwise over the course of 90 minutes, with vigorous stirring, in such a way that the pH value of the reaction mixture is constantly kept in the range between 7.5 and 8.5. Thereafter, 1 N NaOH is added in such a way that a pH value of the reaction mixture of about 8.0 is maintained, and persists as the final value. Thereafter, the organic phase is separated off, washed with 100 ml of water and concentrated at room temperature. 39 g (99% of theory) of 2-(3,5-dichloro-4-hydroxyphenyl)-2-(3,5-dichloro-4-cyanatophenyl)-propane are obtained as the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04060541 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-13f3c81c6ca146db9978f7c0560d11dd |
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| Source note | uspto-grants-1977_11 |
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