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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257171Generated: October 26, 2026

2-(Methylamino)ethanol → 2-(Benzooxazol-2-yl-methyl-amino)-ethanol

https://huagongshe.com/reaction/257171

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methylamino)ethanolHCID 8016—
Reactant2-ChlorobenzoxazoleHCID 11986—
SolventTetrahydrofuranHCID 8028—
Product2-(Benzooxazol-2-yl-methyl-amino)-ethanolHCID 10241663—

Reaction Steps

A solution of 2-chlorobenzoxazole (15.4 g) in dry tetrahydrofuran (50 ml) was added dropwise to an ice cooled solution of 2-methylaminoethanol (15.0 g) in dry tetrahydrofuran (100 ml) with stirring and protection from atmospheric moisture. The mixture was stirred at 0° C. for 1 hour, allowed to warm to room temperature and stirred for a further 2 hours. The solvent was removed under reduced pressure, the product was dissolved in ethyl acetate (200 ml) and washed with brine (2×150 ml). The organic layer was dried (MgSO4), filtered and the solvent evaporated. Chromatography of the residue on silica-gel in dichloromethane gave the title compound (mp 62°-3° C.) which was used in Preparation 3 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260445
Source datasetuspto-grants-1993_11
ORD IDord-ac8ef7ba26d34456bba906b22b6ab87b
Source noteuspto-grants-1993_11