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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557449Generated: October 29, 2026

5-(N-formyl-N-methylamino-methyl)-2-nitrobenzoic acid methyl ester → 2-amino-5-(N-formyl-N-methylamino-methyl)benzoic acid methyl ester

https://huagongshe.com/reaction/557449

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(N-formyl-N-methylamino-methyl)-2-nitrobenzoic acid methyl esterHCID 58018325—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-amino-5-(N-formyl-N-methylamino-methyl)benzoic acid methyl esterHCID 58018332—

Reaction Conditions

Temperature40 °C

Reaction Steps

There was dissolved, in 34 mL of methanol, 4.47 g of the crude product of 5-(N-formyl-N-methylamino-methyl)-2-nitrobenzoic acid methyl ester, prepare in the step 1, 5% Pd/C (wet product) was added to the solution in an argon gas atmosphere and then hydrogen gas was introduced into the reaction container. The reaction system was stirred at a reaction temperature of 40° C. for 8 hours, the hydrogen gas was replaced with argon gas, 14 mL of methanol was then added to the reaction system and the temperature thereof was raised up to 55° C. The Pd/C catalyst was removed through filtration under reduced pressure, the catalyst was washed with 25 mL of methanol and the resulting filtrate and the wash liquid were maintained at a temperature of 40° C. Water (31 mL) was dropwise added thereto thus separate out solid and the resulting slurry was stirred at 10° C. overnight. The resulting solid was separated from the slurry through filtration under reduced pressure, washed with 7 mL of water and then dried under reduced pressure at 70° C. for 5 hours to give 2.53 g of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058432B2
Source datasetuspto-grants-2011_11
ORD IDord-af374356c08043fca784c60682369f9b
Source noteuspto-grants-2011_11