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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594008Generated: October 31, 2026

P-Phenylenediamine → N1-(4-phenylphthalazin-1-yl)benzene-1,4-diamine

https://huagongshe.com/reaction/594008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-PhenylenediamineHCID 7814—
Reactant1-Chloro-4-phenylphthalazineHCID 272109—
SolventWaterHCID 962—
ProductN1-(4-phenylphthalazin-1-yl)benzene-1,4-diamineHCID 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 numberUS09242961B2
Source datasetuspto-grants-2016_01
ORD IDord-847d28133d3e4a14a30da5c68bf4bed9
Source noteuspto-grants-2016_01