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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1683280Erstellt: 26. Oktober 2026

N,N,N',N'-Tetramethylmethanediamine → 3-Cyanomethyl-5-phenoxyindole

https://huagongshe.com/reaction/1683280

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N,N',N'-TetramethylmethanediamineHCID 5829—
EduktDichloromethaneHCID 6344—
EduktSodium HydroxideHCID 14798—
Edukt5-phenoxy-1H-indoleHCID 11241253—
LösungsmittelAcetyl chlorideHCID 6367—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt3-Cyanomethyl-5-phenoxyindoleHCID 19042886—

Reaktionsschritte

To a cooled (ice bath) solution of bis (dimethylamino)methane (0.34 g) in dichloromethane (25 ml), acetyl chloride was added dropwise over 5 minutes. After stirring for 10 minutes, 5-phenoxyindole (0.51 g) was added and stirring continued for a further one hour at room temperature. The mixture was basified with aqueous 2N sodium hydroxide, brine (50 ml) added and the organic phase separated washed with water (2×50 ml), dried (MgSO4) and the solvent removed at reduced pressure. The residue was dissolved in dimethylformamide (25 ml) and potassium cyanide (0.62 g) and iodomethane (0.61 g) added. After stirring for 48 hours, the mixture was diluted with water (50 ml) and extracted with ethyl acetate (3×50 ml). The combined organic phases were washed with water (4×50 ml), dried (MgSO4) and solvent removed at reduced pressure to give 3-cyanomethyl-5-phenoxyindole (0.57 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05637593
Quelldatensatzuspto-grants-1997_06
ORD IDord-57d367acd9094def968ed276d7b6163b
Quellennotizuspto-grants-1997_06