Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83789Generated: October 26, 2026

6-(4-Nitrophenoxy)-hexanoic acid methyl ester → 6-(4-Aminophenoxy)-hexanoic acid methyl ester

https://huagongshe.com/reaction/83789

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(4-Nitrophenoxy)-hexanoic acid methyl esterHCID 14650295—
CatalystNickelHCID 935—
SolventDimethylformamideHCID 6228—
Product6-(4-Aminophenoxy)-hexanoic acid methyl esterHCID 1465029678.8%

Reaction Steps

Method-A Through a mixture of 6-(4-aminophenoxy)-hexanoic acid hydrochloride 16 (150 g, 578 mmol) in methanol (3 L) was passed dry HCl gas at 10° C. for 1 hour and refluxed for 48 hours. Methanol (1.5 L) was distilled off, ice water (1 L) was added and the pH adjusted to 7.5 with K2CO3. Crude 17 was extracted into chloroform, washed with 5% NaHCO3 solution, then water, and then dried over Na2SO4 and distilled to give 17 (60 g, 43.8%) as a thick brown syrup. Method-B 6-(4-Nitrophenoxy)-hexanoic acid methyl ester 21 (40 g, 149.81 mmol) was dissolved in dimethyl formamide (200 ml) in a pressure vessel. Raney nickel (20 g) was added and the mixture stirred under an atmosphere of hydrogen (4 kg) for 16 hours. Catalyst was removed by filtration and dimethyl formamide distilled off under vacuum. Crude 17 was purified by column chromatography on silica gel using chloroform as eluant to get pure 17 (28 grams, 78.8%) as a thick brown syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846845B2
Source datasetuspto-grants-2014_09
ORD IDord-68d8e3382d704997bd548e91ad074dec
Source noteuspto-grants-2014_09