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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057728Generated: October 26, 2026

4-Chloroaniline → 1-(4-Chloroanilino)phthalazine

https://huagongshe.com/reaction/1057728

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanilineHCID 7812—
Reactant1(2H)-PhthalazinoneHCID 8394—
Reactant1-ChlorophthalazineHCID 160793—
Solvent1-ButanolHCID 263—
Product1-(4-Chloroanilino)phthalazineHCID 22741997—

Reaction Steps

30 g (149 mmol) 1-chlorophthalazine (prepared from phthalazone in the manner described under Example 67A.1) and 20 g (157 mmol) 4-chloroaniline are heated in 630 ml n-butanol for 30 min to 65° C. The crude product is filtered off, washed with ether, taken up in 2 l dichloromethane/methanol 9:1, and washed with sat. NaHCO3 solution and brine. The aqueous phases are extracted three times with dichloromethane/methanol 9:1, the organic phases dried (Na2SO4), and evaporated to a residual volume of ≈50 ml, leading to crystallization of the title compound: m.p.: 211° C.; Anal. calc.(C14H10N3Cl) C, 65.76%; H, 3.94%; N, 16.43%; Cl, 13.86%; found C, 66.02%; H, 3.92%; N, 16.53%; Cl, 13.51%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514974B2
Source datasetuspto-grants-2003_02
ORD IDord-217889a093214a2da0c889e2c0aa920c
Source noteuspto-grants-2003_02