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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380153Generated: October 31, 2026

2-Methyl-3-nitrophenol → 2-Amino-o-cresol

https://huagongshe.com/reaction/1380153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-3-nitrophenolHCID 79579—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-o-cresolHCID 104448—

Reaction Steps

2-Methyl-3-nitrophenol (70 g) in 100 ml of tetrahydrofuran and 400 ml of methanol at room temperature was hydrogenated under 5 psi of hydrogen gas using 3.5 g of 5% palladium on carbon as catalyst. After removal of catalyst by filtration, the filtrate was concentrated to give 56 g of analytically pure 3-amino-2-methylphenol. This aminophenol was then converted to the title compound (7.9 g) using the general method of Example 2, except that the hydrochloride salt was formed by adding hydrogen chloride/dioxane to a methanol solution of the free base. The nmr spectrum and elemental analysis were in agreement with those of title compound prepared by Example 3 (Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04579951
Source datasetuspto-grants-1986_04
ORD IDord-f18a8c348f12494e996a0c21812d76d1
Source noteuspto-grants-1986_04