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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093634Generated: October 31, 2026

Methanol → Methyl 3-amino-5-cyano-2-hydroxybenzoate

https://huagongshe.com/reaction/2093634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl 5-cyano-2-hydroxy-3-nitrobenzoateHCID 68725798—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-amino-5-cyano-2-hydroxybenzoateHCID 6872481278.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 2.71 g of methyl 5-cyano-2-hydroxy-3-nitrobenzoate in a 60 ml of methanol and 40 ml of tetrahydrofuran was added palladium on carbon (500 mg, 10% wet). This suspension was purged with, and stirred under, an atmosphere of hydrogen (via balloon) for 4 h at 50° C. The mixture was then filtered through a plug of Celite, eluting with ethyl acetate (75 ml). The eluent was concentrated in vacuo and the residue was taken up in ethyl acetate (50 ml) and methanol (as needed to dissolve) and was then filtered through a plug of silica gel. The eluent was concentrated in vacuo again and purified via column chromatography using a Biotage Horizon, 65i column, eluting with 1 column volume of 100% hexanes followed by a gradient of 0 to 100% ethyl acetate in hexanes over 10 column volumes, followed by 2 column volumes of 100% ethyl acetate to provide the title compound (1.83 g, 78%). Mass spectrum (ESI) 190.9 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445480B2
Source datasetuspto-grants-2013_05
ORD IDord-e598f3375b364aef9407cea2dc470fea
Source noteuspto-grants-2013_05