HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5567Generated: October 27, 2026
Toluene → 5,5'-Oxy-bis[2-(4-hydroxyphenyl)benzimidazole]
https://huagongshe.com/reaction/5567
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Diphenyl sulfone | HCID 31386 | — |
| Reactant | 3,3',4,4'-Tetraaminodiphenyl ether | HCID 75887 | — |
| Reactant | Phenylparaben | HCID 87250 | — |
| Product | 5,5'-Oxy-bis[2-(4-hydroxyphenyl)benzimidazole] | HCID 136029141 | 30% |
Reaction Steps
A mixture of bis(3,4-diaminophenyl)ether (22.00 g, 0.096 mol), phenyl-4-hydroxybenzoate (41.00 g, 0.194 mol), diphenylsulfone (110.17 g), and toluene (135 ml) was heated under a nitrogen atmosphere for 3.5 hours at 150° C. The toluene was removed and the temperature increased to 250° C. and maintained for 1.5 hours. A vacuum was subsequently applied and the temperature increased to 280° C. and maintained for 1.25 hours. The cooled dark reaction mixture was washed in hot toluene and dried at 110° C. to afford 20.59 g (50% crude yield) of a dark purple powder. The dark solid was extracted with acetone to afford 12.39 g (30% yield) of a tan solid. The endothermic peak as determined by DTA was 317° C. (broad). Analysis calcd. for C26H18N4O3 : C, 71.88%; H, 4.18%; N, 12.90%. Found: C, 71.91%; H, 4.22%; N, 13.06%. The resulting monomer had the following structural formula: ##STR11##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05245044 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-067a37df0148453b970f7e876cfd2a25 |
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| Source note | uspto-grants-1993_09 |
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