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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243547Generated: October 31, 2026

Water → ethyl (4'-(2-[(1S,2R)-2-hydroxy-2-(4-hydroxyphenyl)-1-methylethylamino]ethoxy}-2',6'-dimethylbiphenyl-4-yloxy)acetate

https://huagongshe.com/reaction/2243547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantP-HydroxynorephedrineHCID 6931143—
Reactant[4'-(2-Methanesulfonyloxyethoxy)-2',6'-di-methylbiphenyl-4-yloxy]acetateHCID 86605510—
SolventDimethylformamideHCID 6228—
Productethyl (4'-(2-[(1S,2R)-2-hydroxy-2-(4-hydroxyphenyl)-1-methylethylamino]ethoxy}-2',6'-dimethylbiphenyl-4-yloxy)acetateHCID 86605509—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of [4′-(2-methanesulfonyloxyethoxy)-2′,6′-di -methylbiphenyl-4-yloxy]acetate and 4-((1R,2S)-2-amino-1-hydroxypropyl)phenol (0.71 g) in N,N-dimethylformamide (10 mL) was stirred at 80° C. overnight. Water and ethyl acetate were added to the reaction mixture. The organic layer was separated, washed with water and brine, and dried over an hydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: methylene chloride/methanol=10/1) to afford ethyl (4′-{2-[(1S,2R)-2-hydroxy-2-(4-hydroxyphenyl)-1-methyl-ethylamino]ethoxy}-2′,6′-dimethylbiphenyl-4-yloxy)acetate (0.47 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674938B2
Source datasetuspto-grants-2010_03
ORD IDord-4044d8a781a94800a7b7c7c4d433926f
Source noteuspto-grants-2010_03