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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647856Generated: October 25, 2026

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

https://huagongshe.com/reaction/1647856

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 crystallised 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 numberUS05434184
Source datasetuspto-grants-1995_07
ORD IDord-58c1696bc26e4a2a80f3c0724a2cb416
Source noteuspto-grants-1995_07