HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082165Generated: October 25, 2026
Diazene, (nitrophenyl)phenyl-, (E)- → 2H-Benzotriazole, 2-phenyl-
https://huagongshe.com/reaction/2082165
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diazene, (nitrophenyl)phenyl-, (E)- | HCID 142206 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2H-Benzotriazole, 2-phenyl- | HCID 154096 | — |
Reaction Steps
An o-nitroazobenzene derivative which is selected as a starting material is dissolved in a solvent contained in a reaction vessel into which water, a hydrogenation catalyst and a basic substance are then placed. After the air in the reaction vessel has been replaced by hydrogen, a given amount of hydrogen is charged into the reaction vessel, and the reaction is then allowed to proceed under atmospheric pressure or a given pressure at a temperature of room temperature to 170° C. under agitation. After the reaction has been completed, the catalyst is filtered off, the solvent layer is washed with water, and the solvent is distilled off. The crude product is then purified by recrystallization to obtain the corresponding 2-phenylbenzotriazole as a pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05187289 |
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| Source dataset | uspto-grants-1993_02 |
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| ORD ID | ord-88b7025d56dd4c5e9ade8f6aa450f8fa |
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| Source note | uspto-grants-1993_02 |
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