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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227827Generated: October 25, 2026

P-Phenylenediamine → HCID 57756220, compound

https://huagongshe.com/reaction/227827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-PhenylenediamineHCID 7814—
Reactant1-Chloro-4-phenylphthalazineHCID 272109—
SolventWaterHCID 962—
ProductHCID 57756220HCID 57756220—

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560551B2
Source datasetuspto-grants-2009_07
ORD IDord-6075b051e6e9493d9a18c6d2569faf92
Source noteuspto-grants-2009_07