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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277648Generated: November 1, 2026

Dimethylformamide → HCID 51703, compound

https://huagongshe.com/reaction/1277648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl BromideHCID 6332—
ReactantSodium CarbonateHCID 10340—
Reactant3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indoleHCID 2761023—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 51703HCID 5170367.2%

Reaction Steps

A mixture of 9.91 g of 3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole, 10.6 g of sodium carbonate, 150 ml of dimethylformamide and 4.5 g of ethyl bromide was stirred under an inert atmosphere at 30°-35° C. for 5 hours and was then poured into 1.5 liters of water which caused precipitation. The mixture was stirred for one hour and filtered and the filter was rinsed with water. The recovered product was dried overnight in an oven at 70° C. under reduced pressure in the presence of dehydrating agent to obtain 8.95 g of raw product melting at 205° C. The product was dissolved in 400 ml of refluxing ethyl acetate and the mixture was filtered hot. The filtrate was concentrated to 250 ml and crystallization was effected for one hour. The mixture was filtered and the recovered product was rinsed with ethyl acetate to obtain 6.28 g of 3-(1-ethyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole in the form of yellow crystals melting at 205° C. Concentration of the mother liquors yielded another 1.76 g of product after crystallization for a total yield of 8.04 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04278677
Source datasetuspto-grants-1981_07
ORD IDord-836d46ce5408479d91cb46bf24f186d0
Source noteuspto-grants-1981_07