Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1698912Erstellt: 26. Oktober 2026

methyl 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylate → methyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1698912

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktmethyl 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylateHCID 18322358—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produktmethyl 3-amino-5-(tert-butyl)-1H-pyrrole-2-carboxylateHCID 18322367100%

Reaktionsschritte

A mixture of methyl 5-tert-butyl-3-nitropyrrole-2-carboxylate (0.014 g, 0.062 mmol) and 10% Pd/C (3 mg) in dry MeOH (1 mL) was successively evacuated and purged with H2 three times, then shaken under an atmosphere of H2 (35 psi) for 1 h, diluted with CH2Cl2 and filtered through a pad of Celite®. The filtrate was concentrated under reduced pressure to give methyl 3-amino-5-tert-butylpyrrole-2-carboxylate as a bright yellow oil (0.012 g, 100%). 1H NMR (CDCl3) δ1.26 (s, 9H), 3.82 (s, 3H), 5.52 (d, J=2.8 Hz, 1H), 7.89 (br s, 2H). This material was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06344476B1
Quelldatensatzuspto-grants-2002_02
ORD IDord-9ed61ba318064bc58cbbdf6a8ad0925c
Quellennotizuspto-grants-2002_02