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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305630Generated: November 1, 2026

Methyl 3-methyl-4-(2-methoxy-5-nitrophenoxy)butyrate → Methyl 3-methyl-4-(2-methoxy-5-aminophenoxy)butyrate

https://huagongshe.com/reaction/2305630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-methyl-4-(2-methoxy-5-nitrophenoxy)butyrateHCID 18433387—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 3-methyl-4-(2-methoxy-5-aminophenoxy)butyrateHCID 11322746—

Reaction Steps

At ambient temperature a rapidly stirred solution of methyl 3-methyl-4-(2-methoxy-5-nitrophenoxy)butyrate(400 mg) in methanol (20 mL) containing 10% palladium on carbon (40 mg) was exposed to an atmosphere of hydrogen. When uptake of hydrogen had ceased the solution was filtered and the filter cake washed with methanol. The combined filtrates were evaporated to dryness under reduced pressure, to give methyl 3-methyl-4-(2-methoxy-5-aminophenoxy)butyrate as an oil. (317 mg) m/Z 254(M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441012B1
Source datasetuspto-grants-2002_08
ORD IDord-3f77f4683d644ee1a3028b3cc4762386
Source noteuspto-grants-2002_08