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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368036Generated: October 29, 2026

2-Amino-4-methoxyphenol → 5-Methoxy-2-(3-trifluoromethylphenyl)-benzoxazole

https://huagongshe.com/reaction/1368036

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-methoxyphenolHCID 1419108—
ReactantEthyl 3-(trifluoromethyl)benzene-1-carboximidate hydrochlorideHCID 2730239—
SolventTetrahydrofuranHCID 8028—
Product5-Methoxy-2-(3-trifluoromethylphenyl)-benzoxazoleHCID 12135412—

Reaction Steps

A solution of compound 13 and compound 12 (850 mg, 6.13 mmol) in THF (10 mL) was heated to reflux and allowed to stir overnight. The reaction mixture was allowed to cool and the THF evaporated (in vacuo). The residue was dissolved in ethyl acetate and washed with water. The organic layer was dried over MgSO4 and treated with activated carbon Norit A. The mixture was filtered through Celite 521, and evaporated (in vacuo) and the residue was purified using column chromatography (20% Ethyl acetatelhexanes) to afford compound 10 as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573264B1
Source datasetuspto-grants-2003_06
ORD IDord-55970c53ec7b484b9b92b112f2271ed2
Source noteuspto-grants-2003_06