HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439535Generated: October 26, 2026
Sodium Carbonate → 1-(4-Hydroxyphenyl)-1-(4-cyanatophenyl)-cyclohexane
https://huagongshe.com/reaction/1439535
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Cyanogen Chloride | HCID 10477 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,1-Bis(4-hydroxyphenyl)cyclohexane | HCID 232446 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Hydroxyphenyl)-1-(4-cyanatophenyl)-cyclohexane | HCID 21395867 | 99% |
Reaction Steps
86.8 g (0.1 mol) of 1,1-bis-(4-hydroxyphenyl)-cyclo hexane are suspended in 500 ml of water and 300 ml of methylene chloride at about 0° to 3° C. 20 ml (0.4 mol) of cyanogen chloride are added to this suspension and a solution of 10.6 g (0.1 mol) of Na2CO3 in 50 ml of water is added dropwise over the course of 90 minutes at the same temperature, with vigorous stirring, in such a way that a pH value between 7.5 and 8.5 is maintained in the reaction mixture. Thereafter, 1 N NaOH is added at 0° C in such a way that the abovementioned pH value is maintained, and persists as the final value. Thereafter, the organic phase is separated off and washed with 50 ml of water and the solvent is stripped off at room temperature. 29 g (99% of theory) of 1-(4-hydroxyphenyl)-1-(4-cyanatophenyl)-cyclohexane are thus obtained.
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-2448ea548d0c4864876da647f0934506 |
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| Source note | uspto-grants-1977_11 |
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