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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403565Generated: October 29, 2026

Ammonium formate → Methyl 2-amino-5-((((tert-butoxy)carbonyl)amino)methyl)benzoate

https://huagongshe.com/reaction/403565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantMethyl 5-tert-butoxycarbonylaminomethyl-2-nitrobenzoateHCID 19698365—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductMethyl 2-amino-5-((((tert-butoxy)carbonyl)amino)methyl)benzoateHCID 6010304081.1%

Reaction Steps

A mixture of 0.273 g of methyl 5-{[(tert-butoxycarbonyl)amino]methyl}-2-nitrobenzoate, 0.166 g of ammonium formate and 0.094 g of Pd/C (10%) in 10 ml of EtOH purged beforehand with nitrogen is irradiated under a microwave field at 120° C. for 5 min. The mixture is filtered and the filtrate is evaporated under reduced pressure. The residue is chromatographed on silica gel, elution being carried out with an AcOEt/heptane mixture, (5/95, v/v) as far as (30/70, v/v), to give 0.2 g of the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748441B2
Source datasetuspto-grants-2014_06
ORD IDord-8eb2cfad2add4dbdb74844f9f7c7367b
Source noteuspto-grants-2014_06