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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611492Generated: October 26, 2026

4-(5-Nitro-thiophen-2-yl)-butyric acid methyl ester → 4-(5-Amino-thiophen-2-yl)-butyric acid methyl ester

https://huagongshe.com/reaction/1611492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(5-Nitro-thiophen-2-yl)-butyric acid methyl esterHCID 69233400—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product4-(5-Amino-thiophen-2-yl)-butyric acid methyl esterHCID 6923556266.2%

Reaction Steps

A mixture of 4-(5-nitro-thiophen-2-yl)-butyric acid methyl ester (2.29 g, 10.0 mmol) and palladium hydroxide (500 mg, 20% on carbon) in 30 mL of ethyl acetate and 30 mL of methanol is hydrogenated at 50 psi for 48 hours. The reaction mixture is filtered and concentrated. The residue is purified by flash column chromatography eluting with 1:3 ethyl acetate:hexane to provide 1.32 g of 4-(5-amino-thiophen-2-yl)-butyric acid methyl ester as a dark oil; 1H NMR (DMSO-d6) δ 1.74 (m, 2H), 2.38 (m, 2H), 2.54 (m, 2H), 3.59 (s, 3H), 5.66 (d, J=3 Hz, 1H), 6.24 (d, J=3 Hz, 1H); MS 200.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06987116B2
Source datasetuspto-grants-2006_01
ORD IDord-93728a921a6f4cff8cd5aac40a9f16f2
Source noteuspto-grants-2006_01