Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480712Generated: October 29, 2026

Pyridine → Ethyl 2-(3-Aminocarbonylmethylphenoxy)-2-methylpropionate

https://huagongshe.com/reaction/480712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAmmonium BicarbonateHCID 14013—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant2-(3-((1-Ethoxy-2-methyl-1-oxopropan-2-yl)oxy)phenyl)acetic acidHCID 18766570—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-(3-Aminocarbonylmethylphenoxy)-2-methylpropionateHCID 18766455—

Reaction Steps

3-(1-Ethoxycarbonyl-1-methylethoxy)phenylacetic acid (532 mg, 0.2 mmol) was dissolved in acetonitrile (3 mL). Subsequently, pyridine (0.1 mL, 1.24 mmol) and ammonium hydrogencarbonate (206 mg, 2.6 mmol) were added thereto, and the mixture was stirred for 10 minutes at room temperature. Thereafter, di-tert-butyl dicarbonate [Boc2O (597.2 mL, 2.6 mmol)] was added thereto, and the mixture was stirred for 14 hours. The reaction mixture was concentrated under reduced pressure, and the resultant concentrate was added to water, followed by extraction with chloroform. Subsequently, washing was performed sequentially with 1M hydrochloric acid and saturated brine. The resultant mixture was subjected to drying over magnesium sulfate, concentration under reduced pressure, and purification by silica gel column chromatography (chloroform/methanol=10/1), whereby the target compound was obtained (524 mg, 0.198 mmol, 98.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653334B1
Source datasetuspto-grants-2003_11
ORD IDord-c2970372a8794d82a4e30ae362601ae9
Source noteuspto-grants-2003_11