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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171402Generated: October 31, 2026

Methyl 2-[(4-nitronaphthalen-1-yl)oxy]acetate → Methyl 2-((4-aminonaphthalen-1-yl)oxy)acetate

https://huagongshe.com/reaction/1171402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-[(4-nitronaphthalen-1-yl)oxy]acetateHCID 59553182—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 2-((4-aminonaphthalen-1-yl)oxy)acetateHCID 5955314290.4%

Reaction Steps

(4-Nitro-naphthalen-1-yloxy)-acetic acid methyl ester (0.90 g) and 10% Pd/C (90 mg) in MeOH (150 ml) is stirred at room temperature under 1 atmosphere of hydrogen for 4 h. The mixture is then filtered through Celite® and evaporated to dryness to provide (4-amino-naphthalen-1-yloxy)-acetic acid methyl ester (0.72 g). MS 232 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829560B2
Source datasetuspto-grants-2010_11
ORD IDord-83aea31b3e8147c49dbede96beb4da31
Source noteuspto-grants-2010_11