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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83782Generated: October 25, 2026

Methyl 2-(4-nitrophenoxy)propanoate → Methyl 2-(4-aminophenoxy)propanoate

https://huagongshe.com/reaction/83782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(4-nitrophenoxy)propanoateHCID 4501947—
CatalystNickelHCID 935—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(4-aminophenoxy)propanoateHCID 2206047186.55%

Reaction Steps

Method-A Through a mixture of 2-(4-aminophenoxy)-propionic acid 9 (240 g, 1.103 mmol) in methanol (4.8 liters) was passed dry HCl gas at 10° C. for 1 hour followed by reflux for 48 hours. Methanol (2.5 liter) was distilled off, ice water (1 liter) was added and the pH was adjusted to 7.5 with K2CO3. Crude 10 was extracted into chloroform, washed with 5% NaHCO3 solution, water, dried over Na2SO4 and distilled to give 10 (80 g, 37.2%) as a brown syrup. Method-B 2-(4-Nitrophenoxy)-propionic acid methyl ester 14 (20 g, 88.88 mmol) was dissolved in dimethyl formamide (100 ml) in a pressure vessel, Raney nickel (20 grams) was added and the mixture stirred under an atmosphere of hydrogen (4 kg) for 6 hours. The catalyst was removed by filtration and the dimethyl formamide distilled off under vacuum. Crude 10 was purified by column chromatography on silica gel using chloroform as eluant to get pure 10 (15 g, 86.55%) as a brown syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846845B2
Source datasetuspto-grants-2014_09
ORD IDord-ce083270d03e4b0487e2c288685bc83c
Source noteuspto-grants-2014_09