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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 230710Erstellt: 24. Oktober 2026

Sodium hydride → HCID 67435148, Verbindung

https://huagongshe.com/de/reaction/230710

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktL-ProlinolHCID 640091—
Edukt3-Chlorothiophene-2-carboxylic acidHCID 701269—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 67435148HCID 6743514811,3%

Reaktionsschritte

To a solution of 3-chlorothiophene-2-carboxylic acid (0.5 g; 6.325 mmol) in dimethylformamide (5 ml) was added 1,1′-carbonyldiimidazole (1.07 g; 6.64 mmol) and the solution stirred at room temperature for 1 h, followed by the addition of (S)-(+)-2-pyrrolidinemethanol (0.655 ml; 6.64 mmol). The reaction was stirred at room temperature overnight whereupon 60% sodium hydride in mineral oil (0.507 g; 12.7 mmol) was carefully added and the mixture was heated slowly to 150° C. with the progress of the reaction being monitored by thin layer chromatography. The reaction was cautiously diluted with water and extracted with ethyl acetate and the organic layer washed with water then dried (Na2SO4) and evaporated to give the crude product. Purification by flash chromatography eluting with 0-10% (v/v) methanol in dichloromethane followed by crystallisation from ethyl acetate-petroleum ether (40-60) afforded the title compound (0.15 g). M.p.: 167-167.5° C.; EIMS: m/z=222.2 [M+H]+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07566778B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-32173633450645a88c95458621e01b51
Quellennotizuspto-grants-2009_07