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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372594Generated: November 2, 2026

Methyl 2-(4-hydroxy-3-nitrophenyl)acetate → Methyl 2-(3-amino-4-hydroxyphenyl)acetate

https://huagongshe.com/reaction/1372594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(4-hydroxy-3-nitrophenyl)acetateHCID 1473109—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 2-(3-amino-4-hydroxyphenyl)acetateHCID 1475136—

Reaction Steps

Methyl 4-hydroxy-3-nitrophenylacetate (2.15 g, 10.1 mmol) and 5% palladium/carbon (2.15 g) were suspended in methanol (100 ml). The resulting suspension was subjected to catalytic hydrogenation for 20 hours under stirring at room temperature and normal pressure. The catalyst was then filtered off from the reaction mixture. The filtrate was distilled under reduced pressure to remove the solvent, whereby the title compound (1.72 g, 93%) was obtained as a brown solid (this compound was provided for the subsequent reaction without further purification).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-cdeb7798aac34171a7d3e2ae329df2a6
Source noteuspto-grants-2007_01