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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49896Generated: October 29, 2026

4-Chloroaniline → HCID 6326419, compound

https://huagongshe.com/reaction/49896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloroanilineHCID 7812—
ReactantSodium CarbonateHCID 10340—
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantPhosphorus oxide (P4O10)HCID 14812—
ReactantHCID 10777138HCID 10777138—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 6326419HCID 6326419—

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 910 mg (6.36 mmol) phosphorus pentoxide, 876 mg (6.36 mmol) triethylamine hydrochloride, and 812 mg (6.36 mmol) 4-chloroaniline is heated at 200° C. until a homogeneous melt has formed. To the melt, 400 g (1.59 mmol) 4-[(2-methyl-pyridin-4-yl)-methyl]-1(2H)-phthalazinone is added and the reaction mixture stirred for a further 16 h at 200° C. The cooled reaction mixture is distributed with thorough stirring and use of an ultrasonic bath between a dichloromethane/methanol mixture (about 20:1) and saturated aqueous sodium carbonate solution. The organic phase washed with water and brine is dried over anhydrous sodium sulfate, evaporated under vacuum, and the residue purified by means of flash chromatography on silica gel with particle size 0.04-0.06 mm, using an acetate/methanol mixture (19:1). Title compound is obtained after evaporation of the product-containing fractions under vacuum and crystallization of the residue from acetonitrile; m.p. 158-159° C.; ESI-MS: (M+H)+=361. The starting material is prepared as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710047B2
Source datasetuspto-grants-2004_03
ORD IDord-16b3b8617bca4dd182de9a05e435f45d
Source noteuspto-grants-2004_03