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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365712Generated: November 1, 2026

2-(3-nitro-1H-pyrazol-1-yl)ethanol → 2-(3-Amino-1H-pyrazol-1-yl)ethan-1-ol

https://huagongshe.com/reaction/2365712

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-nitro-1H-pyrazol-1-yl)ethanolHCID 16394849—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(3-Amino-1H-pyrazol-1-yl)ethan-1-olHCID 21279853107.9%

Reaction Steps

A solution 2-(3-nitro-pyrazol-1-yl)-ethanol (3.46 g, 22.02 mmol) in ethanol (40 mL) was placed in a Parr shaker bottle and treated with 10% palladium on carbon (350 mg). The bottle was then put on the Parr shaker and charged with hydrogen to 50 psi and let shake for 1 h. After this time, the reaction mixture was filtered through celite and the celite washed with ethanol. The filtrate was then concentrated in vacuo and azeotroped with acetonitrile and then chloroform to afford 2-(3-amino-pyrazol-1-yl)-ethanol (3.02 g, >quant.) as a light yellow viscous oil: 1H NMR (300 MHz, DMSO-d6 δ ppm 7.26 (d, J=1.83 Hz, 1H), 5.34 (d, J=2.20 Hz, 1H), 4.76 (t, J=5.31 Hz, 1H), 4.50 (s, 2H), 3.78-3.88 (m, 2H), 3.62 (q, J=5.74 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697705B2
Source datasetuspto-grants-2014_04
ORD IDord-09e9b1cdff5244bc9f16249fa962df3b
Source noteuspto-grants-2014_04