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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036571Generated: October 26, 2026

Methylamine → 2-bromo-N-methyl-3-nitrobenzamide

https://huagongshe.com/reaction/2036571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Bromo-3-nitrobenzoic acidHCID 68452—
ReactantDiisopropylethylamineHCID 81531—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-bromo-N-methyl-3-nitrobenzamideHCID 67433447—

Reaction Steps

To a solution of 2-bromo-3-nitrobenzoic acid (0.974 g, 3.96 mmol) in DMF (3 mL) was added methylamine, 2.0 m solution in tetrahydrofuran (2.97 mL, 5.94 mmol), 1,1′-dimethyltriethylamine (1.38 mL, 7.92 mmol) and (1H-benzo[d]-[1,2,3]triazol-1-yloxy)tripyrrolidin-1-ylphosphonium hexafluorophosphate(V) (2.47 g, 4.75 mmol) and the resulting mixture was stirred at rt for 2 h. The reaction mixture was diluted with EtOAc, washed with water and brine, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel column using DCM/EtOAc-DCM (1:1) as eluent to give 2-bromo-N-methyl-3-nitrobenzamide: LC-MS (ESI) m/z 261.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575183B2
Source datasetuspto-grants-2013_11
ORD IDord-cc6e0d8e9c424a57af304fc3f446ea1c
Source noteuspto-grants-2013_11