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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175557Generated: October 31, 2026

Trifluoroacetic anhydride → 4-((4-Methoxybenzyl)oxy)-6-(trifluoromethyl)quinoline-2-carbonitrile

https://huagongshe.com/reaction/2175557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant4-((4-Methoxybenzyl)oxy)-6-(trifluoromethyl)quinoline-2-carboxamideHCID 58562851—
Product4-((4-Methoxybenzyl)oxy)-6-(trifluoromethyl)quinoline-2-carbonitrileHCID 58562526—

Reaction Steps

A solution of 4-((4-methoxybenzyl)oxy)-6-(trifluoromethyl)quinoline-2-carboxamide (9 g, 24 mmol) from above step B, and TEA (10 mL, 72 mmol) was treated with trifluoroacetic anhydride (4.35 mL, 31.3 mmol) at room temperature and stirred for 2 h (completion of reaction monitored by LCMS). Solvent was removed under vacuum and the residue was purified by recrystallization from EtOAc/Hex to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062048B2
Source datasetuspto-grants-2015_06
ORD IDord-d3f9ec46672a4317ba09c4d3ba98801e
Source noteuspto-grants-2015_06