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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680682Generated: October 30, 2026

2-Chlorobenzoxazole → HCID 12898688, compound

https://huagongshe.com/reaction/1680682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
Reactant4-Fluoro-3-(trifluoromethyl)anilineHCID 75377—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12898688HCID 12898688—

Reaction Steps

To a solution of 17.9 g. (0.1 mole) of 4-fluoro-3-(trifluoromethyl)aniline in 200 ml. of tetrahydrofuran was added dropwise 15.4 g. (0.1 mole) of 2-chlorobenzoxazole in 150 ml. of tetrahydrofuran with vigorous agitation. Following the addition, the reaction mixture was heated on a steam bath under reflux for 16 hours. Then the tetrahydrofuran solvent was removed by distillation under vacuum, and 100 ml. of water was added to the residue. The residue was an oily liquid which solidified on the addition of the water. The residue was removed by filtration and dried in vacuo. The dried residue was dissolved in a minimum amount of warm acetone, and about 200 ml. of water was added to the solution, resulting in the crystallization of the reaction product. The precipitate was filtered and dried and 24.5 g. of 2-[4-fluoro-3-(trifluoromethyl)anilino]benzoxazole having a melting point of 190°-191° C. was recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04275210
Source datasetuspto-grants-1981_06
ORD IDord-9ba38a3b448849509a4d19174418a4db
Source noteuspto-grants-1981_06