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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277646Generated: October 31, 2026

Isopropyl iodide → HCID 3055752, compound

https://huagongshe.com/reaction/1277646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
Reactant3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indoleHCID 2761023—
CatalystSilver(II) oxideHCID 92152—
SolventAcetoneHCID 180—
ProductHCID 3055752HCID 3055752—

Reaction Conditions

Temperature50 °C

Reaction Steps

3.15 g of silver oxide and 2.25 ml of isopropyl iodide were added to a solution of 4.5 g of 3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole in 90 ml of acetone and the mixture was heated at 50° C. for 3 hours and was then cooled. The mixture was filtered and the filtrate was distilled to dryness under reduced pressure. The residue was chromatographed over silica gel and was eluted with a 6-3-1 chloroform-acetone-triethylamine mixture. The fractions were distilled to dryness and the residue was dissoved in 200 ml of refluxing ethyl acetate. The mixture was filtered and the filtrate was concentrated to 150 ml and cooled to 20° C. Crystallization was induced and the mixture was iced overnight and vacuum filtered. The recovered product was washed with ethyl acetate and dried to obtain 3.9 g of 3-(1-propyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole melting at 210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04278677
Source datasetuspto-grants-1981_07
ORD IDord-5e072d81faa545eb9efdd6fb1017947e
Source noteuspto-grants-1981_07