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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43577Generated: October 28, 2026

Methyl 5-methyl-2-(4-nitrophenyl)oxazole-4-carboxylate → Methyl 2-(4-aminophenyl)-5-methyl-1,3-oxazole-4-carboxylate

https://huagongshe.com/reaction/43577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-methyl-2-(4-nitrophenyl)oxazole-4-carboxylateHCID 67548650—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 2-(4-aminophenyl)-5-methyl-1,3-oxazole-4-carboxylateHCID 6840599066.2%

Reaction Steps

The same operation as in Example (95b) was performed using methyl 5-methyl-2-(4-nitrophenyl)-1,3-oxazole-4-carboxylate obtained in Example (97c) (0.75 g, 2.86 mmol), 10% Pd/C (0.3 g) and methanol (10 mL). Purification by silica gel column chromatography (elution solvent: ethyl acetate/hexane=1/2, 1/1, 1/2, 1/4) gave 0.44 g of the title compound as a colorless solid (66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-6759ee8b96bf434dbd4615ca55a464dd
Source noteuspto-grants-2013_09