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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359719Generated: October 25, 2026

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

https://huagongshe.com/reaction/359719

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. 1H NMR δ (CDCl3) 3 30 (3H, s); 3.85 (2H, t); 4.30 (2H, t) 6.80-7.85 (8H, complex); 9.85 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05002953
Source datasetuspto-grants-1991_03
ORD IDord-25643cc84cf149c3bb86d2902d2a3d44
Source noteuspto-grants-1991_03