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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270942Generated: October 31, 2026

2-Aminophenol → 2-(Pyridin-4-yl)-1,3-benzoxazole

https://huagongshe.com/reaction/2270942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminophenolHCID 5801—
Reactant4-PyridinecarboxaldehydeHCID 13389—
SolventAcetic AcidHCID 176—
Product2-(Pyridin-4-yl)-1,3-benzoxazoleHCID 16804—

Reaction Conditions

Temperature100 °C

Reaction Steps

A 500 mg portion of pyridine-4-aldehyde was dissolved in 15 ml of acetic acid, and the solution was mixed with 509 mg of o-aminophenol and stirred with heating at 100° C. for 6 hours. The solvent was concentrated under a reduced pressure, and the residual oily matter was mixed with saturated sodium bicarbonate aqueous solution and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried with magnesium sulfate, and then the solvent was evaporated under a reduced pressure. Thereafter, the thus obtained mixture was purified by a silica gel column chromatography (ethyl acetate:hexane=1:1) to obtain the title compound (90 mg) in light yellow color.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333328B1
Source datasetuspto-grants-2001_12
ORD IDord-73b1b76b601a4b9a96a3c95aba3f73ea
Source noteuspto-grants-2001_12