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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828733Generated: November 1, 2026

4-(Trifluoromethyl)benzoyl chloride → HCID 22057983, compound

https://huagongshe.com/reaction/1828733

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzoyl chlorideHCID 67607—
ReactantHCID 22057974HCID 22057974—
SolventTriethylamineHCID 8471—
ProductHCID 22057983HCID 2205798352%

Reaction Steps

Using an analogous procedure to that described in Example 4, 4-trifluoromethylbenzoyl chloride was reacted with N-(5-amino-2-methylphenyl)-quinoline-6-carboxamide in the presence of triethylamine. The reaction mixture was stirred at ambient temperature for 18 hours and then evaporated. The residue was purified by column chromatography on silica using increasingly polar mixtures of methylene chloride and methanol as eluent. There was thus obtained the title compound in 52% yield; Mass Spectrum: M+H+ 450.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060700B2
Source datasetuspto-grants-2006_06
ORD IDord-cd0c771dd6a54a6ca16a150c8ab4a1f7
Source noteuspto-grants-2006_06