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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683280Generated: October 26, 2026

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

https://huagongshe.com/reaction/1683280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylmethanediamineHCID 5829—
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant5-phenoxy-1H-indoleHCID 11241253—
SolventAcetyl chlorideHCID 6367—
SolventSodium chloride; waterHCID 57417360—
Product3-Cyanomethyl-5-phenoxyindoleHCID 19042886—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637593
Source datasetuspto-grants-1997_06
ORD IDord-57d367acd9094def968ed276d7b6163b
Source noteuspto-grants-1997_06