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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711888Generated: November 2, 2026

2-((2-Methylcyclopropyl)methoxy)-6-nitrobenzonitrile → 2-Amino-6-((2-methylcyclopropyl)methoxy)benzonitrile

https://huagongshe.com/reaction/711888

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((2-Methylcyclopropyl)methoxy)-6-nitrobenzonitrileHCID 66746593—
CatalystPalladiumHCID 23938—
SolventEthanol ethylacetateHCID 21584252—
Product2-Amino-6-((2-methylcyclopropyl)methoxy)benzonitrileHCID 6674690179.1%

Reaction Steps

A solution of 2-((2-methylcyclopropyl)methoxy)-6-nitrobenzonitrile (example 254c) (0.29 g, 1.25 mmol) in EtOAc/EtOH 1:1 (30 mL) was hydrogenated in an H-cube apparatus using 10% Pd/C as catalyst. The solution was evaporated to give 2-amino-6-((2-methylcyclopropyl)methoxy)benzonitrile (0.20 g, 79%) as a yellow oil. MS 203 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181276B2
Source datasetuspto-grants-2015_11
ORD IDord-ba0fb513c5dc40b09bd285c1a908a747
Source noteuspto-grants-2015_11