HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048978Generated: October 31, 2026
1-Chloro-4-nitrobenzene → 2,2'-Bis(4-nitrophenoxy)-1,1'-biphenyl
https://huagongshe.com/reaction/2048978
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloro-4-nitrobenzene | HCID 7474 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (1,1'-Biphenyl)-2,2'-diol | HCID 15731 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,2'-Bis(4-nitrophenoxy)-1,1'-biphenyl | HCID 14344369 | 15% |
Reaction Steps
37.2 g (0.2 mol) of 2,2'-dihydroxy-biphenyl and 63 g (0.4 mol) of p-nitrochlorobenzene are dissolved in 160 ml of dimethylsulphoxide (DMSO) in a sulphonation flask and the solution is warmed to 80° C. A solution of 26.4 g (0.4 mol) of 85% strength potassium hydroxide in 20 ml of water is then added dropwise, whilst stirring, and the reaction solution is subsequently further stirred for 3 hours at 100°-110° C. After cooling, the reaction solution is poured into ice water and the resulting precipitate is washed several times with water. The resulting crude product is then dried for 20 hours under a high vacuum at 70° C. and unconverted nitrochlorobenzene sublimes away during drying. The residue is recrystallised twice from ethanol. 12.4 g (15% of theory) of 2,2'-di-(p-nitrophenoxy)-biphenyl are obtained in the form of slightly yellowish crystals; melting point 158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04196144 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-44b22f45f1344b26ba5f8d37cd789667 |
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| Source note | uspto-grants-1980_04 |
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