Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277371Generated: November 1, 2026

1-((4-(2-Fluoro-4-nitrophenoxy)quinolin-7-yl)oxy)-2-methylpropan-2-ol → 1-((4-(4-Amino-2-fluorophenoxy)quinolin-7-yl)oxy)-2-methylpropan-2-ol

https://huagongshe.com/reaction/2277371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((4-(2-Fluoro-4-nitrophenoxy)quinolin-7-yl)oxy)-2-methylpropan-2-olHCID 68194028—
ReactantHCID 178526052HCID 178526052—
CatalystPalladiumHCID 23938—
SolventOxolane--water (1/1)HCID 21881883—
Product1-((4-(4-Amino-2-fluorophenoxy)quinolin-7-yl)oxy)-2-methylpropan-2-olHCID 6819400387.6%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a mixture of 1-((4-(2-fluoro-4-nitrophenoxy)quinolin-7-yl)oxy)-2-methylpropan-2-ol (10.04 g, 27 mmol) and HCOOK (15.87 g, 189 mmol) in THF/H2O (54 mL, THF/H2O=4:1) was added catalytic amount of Pd/C (5%, 53%˜55% water content, w/w). The reaction was stirred at 45° C. for 5 hours, and then diluted with THF/H2O (40 mL, v/v=1:1). The resulted mixture was filtered and the filtrate was concentrated in vacuo. The residue was washed with EtOH/H2O (30 mL×3, v/v=5:1), and dried in vacuo at 45° C. for 24 hours to give the title compound as a light gray solid (8.1 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133162B2
Source datasetuspto-grants-2015_09
ORD IDord-11c363c1d4aa4f64bb0d59af923941f1
Source noteuspto-grants-2015_09