Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129348Erstellt: 24. Oktober 2026

Dimethylformamide → Ethyl 1-tetradecylpyrrole-3-carboxylate

https://huagongshe.com/de/reaction/129348

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktMyristyl bromideHCID 8208—
EduktSodium hydrideHCID 24758—
EduktEthyl 1H-pyrrole-3-carboxylateHCID 13070719—
LösungsmittelWaterHCID 962—
ProduktEthyl 1-tetradecylpyrrole-3-carboxylateHCID 1502335494,3%

Reaktionsschritte

To dry dimethylformamide (DMF) (15 ml) was added 0.84 g (21 mmol) of sodium hydride (60% oil dispersion), and then 2.78 g (20 mmol) of ethyl pyrrole-3-carboxylate was added portionwise thereto under ice-cooling. After stirring at room temperature for 10 minutes, 6.65 g (24 mmol) of bromotetradecane was added dropwise under ice-cooling. The mixture was stirred for 3.5 hours at room temperature, and then 30 ml of water was added thereto. The resulting mixture was extracted with 70 ml of ethyl acetate, washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. After removing the solvent, the remaining oil was purified by subjecting it to column chromatography over silica gel (eluent: ethyl acetate/hexane=1/20-1/10) to obtain 6.33 g (89.0% yield) of ethyl 1-tetradecylpyrrole-3-carboxylate as white crystals, m.p. 32°-33° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE035096
Quelldatensatzuspto-grants-1995_11
ORD IDord-c0ba77a295b6402a95171267e1c0cb30
Quellennotizuspto-grants-1995_11