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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2036571Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/2036571

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylamineHCID 6329—
EduktTetrahydrofuranHCID 8028—
Edukt2-Bromo-3-nitrobenzoic acidHCID 68452—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-bromo-N-methyl-3-nitrobenzamideHCID 67433447—

Reaktionsschritte

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]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08575183B2
Quelldatensatzuspto-grants-2013_11
ORD IDord-cc6e0d8e9c424a57af304fc3f446ea1c
Quellennotizuspto-grants-2013_11