Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1825747Erstellt: 26. Oktober 2026

Dimethylformamide → Methyl 3-formyl-1H-indole-7-carboxylate

https://huagongshe.com/reaction/1825747

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPhosphorus oxychlorideHCID 24813—
EduktMethyl indole-7-carboxylateHCID 676694—
EduktDMF Phosphorus oxychlorideHCID 13765457—
Lösungsmittel1,2-DichloroethaneHCID 11—
ProduktMethyl 3-formyl-1H-indole-7-carboxylateHCID 76296593%

Reaktionsschritte

To a stirred mixture of phosphorus oxychloride-dimethylformamide in anhydrous 1,2-dichloroethane (prepared by the slow addition of phosphorus oxychloride (0.43 ml, 4.6 mmol) to anhydrous DMF (0.35 ml, 4.6 mmol) in anhydrous 1,2-dichloroethane (6 ml) cooled below 5° C.) a solution of 7-methoxycarbonylindole (0.69 g, 4 mmol) in anhydrous 1,2-dichloroethane (6 ml) was dropwise below 5° C. The mixture was stirred at room temperature for 2 h and then was heated at 50° C. for 30 minutes. After cooling, the precipitate was filtered off and washed with 1,2-dichloroethane. This precipitate was suspended in aq Na2CO3 10% (30 ml) and stirred at room temperature for 20 minutes; dichloromethane was added and stirring was continued 10 minutes more. The organic phase was separated and the aqueous phase was extracted with dichloromethane. The combined organic extracts were washed with brine, dried over anhydrous magnesium sulfate and evaporated to yield 0.75 g (93%) of the entitled product. Mp: 153–4° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07049312B1
Quelldatensatzuspto-grants-2006_05
ORD IDord-1b6c9aa600274133865828d9e9ab2640
Quellennotizuspto-grants-2006_05