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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374539Generated: October 25, 2026

Methanol → Methyl 4-[2-(2-hydroxy-2-phenylethylamino)ethoxy]phenylacetate hydrochloride

https://huagongshe.com/reaction/374539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant4-[2-(2-Hydroxy-2-phenylethylamino)ethoxy]phenylacetamide hydrochlorideHCID 18997240—
ProductMethyl 4-[2-(2-hydroxy-2-phenylethylamino)ethoxy]phenylacetate hydrochlorideHCID 18997237—

Reaction Steps

4-[2-(2-Hydroxy-2-phenylethylamino)ethoxy]phenylacetamide hydrochloride (2.5 g) was heated under reflux in methanol (50 ml) containing concentrated sulphuric acid (1.5 ml) for 24 hours. The mixture was cooled and the solvent evaporated under reduced pressure. The residue was partitioned between dichloromethane (150 ml) and 5% NaHCO3 solution (150 ml). The organic layer was separated and washed successively with 5% NaHCO3 solution (20 ml) and water (20 ml), dried over MgSO4 and then the solvent was removed under reduced pressure. The residue was dissolved in methyl acetate (40 ml) and treated with a solution of ether saturated with hydrogen chloride. The precipitated solid was crystallized from a mixture of methanol and methyl acetate to give methyl 4-[2-(2-hydroxy-2-phenylethylamino)ethoxy]phenylacetate hydrochloride (1.8 g), m.p. 169°-171° C.; microanalysis: found C, 62.5; H, 6.6; N, 3.8; Cl, 9.7%; required for C19H24ClNO 4 : C, 62.4; H, 6.6; N, 3.8; Cl, 9.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05480910
Source datasetuspto-grants-1996_01
ORD IDord-02d7da2c1dc9499ba54e1ef61bc43377
Source noteuspto-grants-1996_01