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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257170Generated: October 25, 2026

4-Hydroxybenzaldehyde → 4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzaldehyde

https://huagongshe.com/reaction/257170

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant2-(Benzooxazol-2-yl-methyl-amino)-ethanolHCID 10241663—
SolventTetrahydrofuranHCID 8028—
Product4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzaldehydeHCID 10040213—

Reaction Steps

To a solution of 2-[N-methyl-N-(2-benzoxazolyl) amino]ethanol (9.6 g), triphenylphosphine (13.1 g) and 4-hydroxybenzaldehyde (6.1 g) in dry tetrahydrofuran (150 ml) was added dropwise a solution of diethyl azodicarboxylate (9.0 g) in dry tetrahydrofuran (30 ml), under a blanket of nitrogen with stirring at room temperature. The solution was stirred overnight at room temperature following which the solvent was removed under reduced pressure. The residue was dissolved in diethyl ether (300 ml), filtered and the ether solution was washed with dilute sodium hydroxide solution (200 ml), saturated brine (200 ml), dried (MgSO4), filtered and the solvent evaporated. The title compound (mp 97°-98° C.) was obtained after chromatography on silica-gel, eluting with dichloromethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260445
Source datasetuspto-grants-1993_11
ORD IDord-c7b0f98e6b27484d8b7cb8160d65ddb3
Source noteuspto-grants-1993_11