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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495108Generated: October 25, 2026

3-(4-Methoxy-phenoxy)-propylamine → butyl (R)-2-(3-(((3-(4-methoxyphenoxy)propyl)amino)methyl)phenoxy)butanoate

https://huagongshe.com/reaction/495108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Methoxy-phenoxy)-propylamineHCID 3152109—
ReactantSodium borohydrideHCID 4311764—
Reactantn-butyl (R)-2-(3-formylphenoxy)butyrateHCID 11846216—
SolventMethanolHCID 887—
Productbutyl (R)-2-(3-(((3-(4-methoxyphenoxy)propyl)amino)methyl)phenoxy)butanoateHCID 57552765—

Reaction Steps

3-(4-Methoxyphenoxy)propylamine (34 mg) was dissolved in methanol (3 mL), and a solution (2 mL) of n-butyl (R)-2-(3-formylphenoxy)butyrate (50 mg) in methanol was added thereto under stirring at room temperature. The mixture was further stirred at 80° C. for 12 hours. Subsequently, an aqueous solution (0.5 mL) of sodium borohydride (7 mg) was added to the solution at room temperature, and the mixture was stirred for 30 minutes. The reaction solution was concentrated under reduced pressure, and chloroform was added to the concentrated product. The formed organic layer was washed with water. The washed organic layer was dried over sodium sulfate anhydrate, and concentrated under reduced pressure, to thereby yield 81 mg of a pale yellow, oily substance. The entirety of the substance was employed in the following reaction without any further treatment.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538242B2
Source datasetuspto-grants-2009_05
ORD IDord-327652398a9a490d921bd1883f59e10a
Source noteuspto-grants-2009_05