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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366610Generated: October 27, 2026

(3,4-Dimethoxyphenyl)(3-nitrophenyl)methanone → (3-Aminophenyl)(3,4-dimethoxyphenyl)methanone

https://huagongshe.com/reaction/366610

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3,4-Dimethoxyphenyl)(3-nitrophenyl)methanoneHCID 10803185—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product(3-Aminophenyl)(3,4-dimethoxyphenyl)methanoneHCID 1056308738.9%

Reaction Steps

To a solution of 3,4-dimethoxy-3'-nitrobenzophenone (0.5 g, 1.7 mmol) in 40 mL of ethyl acetate was added 0.05 g of 10% palladium on carbon catalyst. The mixture was hydrogenated in a Parr-Shaker apparatus at 55-60 psi of hydrogen for 1.5 hours. The reaction mixture was filtered through celite and the filtrate was concentrated in vacuo to afford the crude product. The crude product was purified by flash column chromatography (silica gel, 10% ethyl acetate/methylene chloride) to afford 0.17 g (38%) of the product as a yellow solid: mp 157-175° C.; 1H NMR (CDCl3) δ 7.56-6.80 (m, 7 H); 3.95 (s, 3 H), 3.94 (s, 3 H); 13C NMR (CDCl3) δ 195.7, 152.9, 148.9, 146.4, 139.3, 130.3, 128.9, 125.4, 120.1, 118.4, 115.6, 112.1, 109.7, 56.0, 56.0; Anal. Calcd for C15H15NO3. Theoretical: C, 70.02; H, 5.88; N, 5.44. Found: C, 70.00; H, 6.10; N, 5.13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130226
Source datasetuspto-grants-2000_10
ORD IDord-c76f0797ae404476baeb892b6a605262
Source noteuspto-grants-2000_10