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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408481Generated: October 31, 2026

4-(Trifluoromethoxy)aniline → HCID 68626825, compound

https://huagongshe.com/reaction/1408481

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethoxy)anilineHCID 600848—
ReactantMethyl 4-chloroquinazoline-7-carboxylateHCID 17750389—
Solvent(+-)-2-ButanolHCID 6568—
ProductHCID 68626825HCID 6862682591%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of methyl 4-chloroquinazoline-7-carboxylate (610 mg, 2.75 mmol) in sec-BuOH (5 mL) was added 4-trifluoromethoxyaniline (535.5 mg, 3.02 mmol) at room temperature. The mixture was heated at 100° C. and stirred for 2 h. The solvent was evaporated and the compound was crystallized from CHCl3 and Et2O mixture (3:1). The white crystals were collected by filtration and washed with Et2O. (890 mg, 91% Yield). MS m/z 364.10 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921336B2
Source datasetuspto-grants-2014_12
ORD IDord-1f2a37b24b834064aa176ef473e52b7b
Source noteuspto-grants-2014_12