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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49912Generated: October 25, 2026

Benzoyl chloride → HCID 178509345, compound

https://huagongshe.com/reaction/49912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1-(4-Chloroanilino)phthalazineHCID 22741997—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178509345HCID 178509345—

Reaction Steps

Under N2 atmosphere, first 164 mg (1.2 mmol) anhydrous aluminium chloride is added to 12.6 g (49.3 mmol) 1-(4-chloroanilino)phthalazine in 90 ml dichloromethane, followed by 12.3 ml (98.6 mmol) trimethylsilyl cyanide. Finally, 11.5 ml (98.6 mmol) benzoyl chloride is added under ice cooling and stirred for 3 h at RT. The suspension is poured onto 0.6 ml water, filtered off, washed with water, and dried. Mixing in 150 ml boiling ethanol yields pure title compound: m.p.: 201-202° C.; Anal. calc.(C22H15N4ClO) C, 68.31%; H, 3.91%; N, 14.48%, Cl, 9.16%. found C, 68.03%; H, 3.89%; N, 14.22%, Cl, 9.42%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710047B2
Source datasetuspto-grants-2004_03
ORD IDord-4f563b29aff94c62bab9fc1f48d41eee
Source noteuspto-grants-2004_03