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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43612Generated: October 29, 2026

Methyl 2-(3-methoxy-4-nitrophenyl)-5-methyl-1,3-oxazole-4-carboxylate → Methyl 2-(4-amino-3-methoxyphenyl)-5-methyl-1,3-oxazole-4-carboxylate

https://huagongshe.com/reaction/43612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(3-methoxy-4-nitrophenyl)-5-methyl-1,3-oxazole-4-carboxylateHCID 68405823—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 2-(4-amino-3-methoxyphenyl)-5-methyl-1,3-oxazole-4-carboxylateHCID 67549647100.9%

Reaction Steps

The same operation as in Example (95b) was performed using methyl 2-(3-methoxy-4-nitrophenyl)-5-methyl-1,3-oxazole-4-carboxylate obtained in Example (105c) (0.75 g, 2.57 mmol), 10% Pd/C (0.2 g) and methanol (20 mL), to obtain 0.68 g of the title compound as a yellow solid (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-7011432aa0084d8c816096b69f86cb54
Source noteuspto-grants-2013_09