HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227827Generated: October 25, 2026
P-Phenylenediamine → HCID 57756220, compound
https://huagongshe.com/reaction/227827
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Phenylenediamine | HCID 7814 | — |
| Reactant | 1-Chloro-4-phenylphthalazine | HCID 272109 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57756220 | HCID 57756220 | — |
Reaction Steps
Benzene-1,4-diamine (0.337 g, 3.12 mmol) and 1-chloro-4-phenylphthalazine (0.500 g, 2.08 mmol) were treated with 7.5 mL 2-BuOH in a sealed tube and heated to 110° C. The reaction quickly became a solid, yellow mass. After several hours, the reaction was cooled and diluted with water. The slurry was then partitioned between DCM and 1N NaOH. The aqueous layer was extracted into DCM (2×). The combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The resulting material was purified by silica gel chromatography, ISCO, 40 g, 0-10% MeOH/MC to give N1-(4-phenylphthalazin-1-yl)benzene-1,4-diamine as an orange-brown solid. MS m/z=313 [M+H]+. Calc'd for C20H16N4: 312.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560551B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-6075b051e6e9493d9a18c6d2569faf92 |
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| Source note | uspto-grants-2009_07 |
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