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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070354Generated: November 3, 2026

3-(2-Methyl-5-nitrophenyl)furan → HCID 60098266, compound

https://huagongshe.com/reaction/2070354

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Methyl-5-nitrophenyl)furanHCID 60098081—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 60098266HCID 6009826698%

Reaction Steps

A suspension of 4-methyl-3-(3-furyl) nitrobenzene 1 (470 mg, 2.31 mmol) and 10% Pd/C (245 mg, 0.23 mmol) in methanol (10 mL) was placed under an H2 atmosphere and the resulting reaction was maintained overnight at rt. The reaction mixture was filtered through Celite and the remaining solids were washed with EtOAc. The combined organic portions were concentrated to provide 400 mg (2.26 mmol, 98%) of an amber residue as 2: LCMS m/z 178.2 (MH+), tR=1.53 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299108B2
Source datasetuspto-grants-2012_10
ORD IDord-cb4aa0a257354b09840f12d937ac2682
Source noteuspto-grants-2012_10