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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 515864Erstellt: 24. Oktober 2026

Methyl iodide → Ethyl 1,2-dimethyl-1H-pyrrole-3-carboxylate

https://huagongshe.com/de/reaction/515864

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
EduktEthyl 2-methyl-3-pyrrolecarboxylateHCID 136747—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktEthyl 1,2-dimethyl-1H-pyrrole-3-carboxylateHCID 12211514—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 10 g of ethyl 2-methyl-1H-pyrrole-3-carboxylate (65.3 mmol) and 8.95 mL (130.6 mmol) of methyl iodide in 70 mL of dimethylformamide placed at 0° C. there are added, in three portions, 2.61 g (65.3 mmol) of sodium hydride (NaH) 60% . The batch is then stirred at 0° C. for 1 hour. Then, the reaction mixture is hydrolysed by the addition of 420 mL of ice-cold water. The reaction mixture is then diluted with ethyl acetate, successively washed with 0.1M aqueous hydrochloric acid (HCl) solution, saturated aqueous LiCl solution and then brine. The organic phase is then dried over MgSO4, filtered, concentrated to dryness and purified by chromatography over silica gel (petroleum ether/AcOEt gradient).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09108983B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-527b8670a95e40e989aab6cfe6fb9720
Quellennotizuspto-grants-2015_08