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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266942Generated: October 26, 2026

Methyl 3-methoxy-5-nitrobenzoate → Methyl 3-amino-5-methoxybenzoate

https://huagongshe.com/reaction/2266942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-methoxy-5-nitrobenzoateHCID 877382—
ReactantAmmonium formateHCID 2723923—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 3-amino-5-methoxybenzoateHCID 1183004698.2%

Reaction Steps

2 g (9.5 mmol) methyl 3-methoxy-5-nitrobenzoate (7) were dissolved in 50 mL methanol by heating, then 0.3 g Pd/C (10%) were added under a stream of nitrogen, followed by 2.99 g (47.5 mmol) ammonium formate. The mixture was refluxed for 3 h, then stirred overnight at r.t.. The clear layer above the catalyst was decanted off portionwise and filtered through a syringe filter. The catalyst that remained in the flask was washed twice with methanol during this procedure. After concentration, 1.69 g of a brown solid were obtained, which were purified by column chromatography (hexanes/ethyl acetate, 7:3). Drying under vacuum afforded 1.25 g (73%) of a colorless solid. 1H NMR (CDCl3) δ 7.00-6.97 (m, 2H), 6.42 (t, J1=2.2 Hz, J2=2.2 Hz), 3.89 (s, 3H, OCH3), 3.80 (s, 3H, OCH3), 3.78 (sb, 2H); 13C NMR (CDCl3) δ 167.13 160.71, 147.49, 131.95, 109.01, 105.71, 104.36, 55.19, 51.880□ESI-MS m/z 314 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858737B2
Source datasetuspto-grants-2010_12
ORD IDord-b83fc1221a1c478abb320c39ad21092c
Source noteuspto-grants-2010_12