HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465289Generated: October 26, 2026
1-Chloro-4-nitrobenzene → HCID 178447844, compound
https://huagongshe.com/reaction/465289
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-4-nitrobenzene | HCID 7474 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178447845 | HCID 178447845 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 178447844 | HCID 178447844 | 76.1% |
Reaction Steps
DMSO (300 ml) and KOH (38.0 g) were added to 1,1-bis(4-hydroxyphenyl)-4-(trans-4-n-propylcyclohexyl)cyclohexane (110.6 g) obtained in the first step, followed by dissolving these together on heating to 65° C., dropwise adding to the solution, a solution of p-chloronitrobenzene (97.8 g) in DMSO (500 ml) at 65° C., reacting the mixture, aging for 5 hours, cooling down to room temperature after completion of the reaction, extracting with dichloromethane, washing with lN-NaOH aqueous solution and further with saturated NaCl aqueous solution till the aqueous solution became neutral, drying over MgSO4, treating by alumina column, distilling off the resulting eluate and recrystallizing the resulting concentrate from a mixed solvent of toluene-acetone to obtain pale yellow crystals of 1,1-bis[4-(4-nitrophenoxy)phenyl]-4-(trans-4-n-propylcyclohexyl)cyclohexane (136.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05152918 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-d21098bb0785447ca17a5d309741bb2e |
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| Source note | uspto-grants-1992_10 |
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