HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593974Generated: October 25, 2026
4-Aminophenol → 4-((4-Phenylphthalazin-1-yl)amino)phenol
https://huagongshe.com/reaction/593974
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | 1-Chloro-4-phenylphthalazine | HCID 272109 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-((4-Phenylphthalazin-1-yl)amino)phenol | HCID 2869168 | — |
Reaction Steps
A pressure bottle was charged with 4-aminophenol (0.453 g, 0.416 mmol), 1-chloro-4-phenylphthalazine (1.00 g, 0.416 mmol) and 16.8 mL of benzene. The bottle was sealed and heated to 100° C. for 25 h. The reaction mixture was concentrated. The crude material was dissolved in methanol and was purified by Gilson reverse phase liquid chromatography, 5-75% ACN/H2O/0.1% TFA over 14 min. The product-containing fractions were combined, brought to basic pH by addition of 1M NaHCO3, and extracted with dichloromethane. The organic portion was dried with MgSO4, filtered and concentrated to provide 4-(4-phenylphthalazin-1-ylamino)phenol as a yellow solid. MS m/z=314 [M+H]+. Calc'd for C20H15N3O: 313.35.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242961B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-a6b1e1ef074f458a8308fbebfeee4f42 |
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| Source note | uspto-grants-2016_01 |
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