Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049884Generated: November 3, 2026

Potassium Iodide → HCID 20344008, compound

https://huagongshe.com/reaction/2049884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantAllyl bromideHCID 7841—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 20343975HCID 20343975—
ReactantHCID 20343976HCID 20343976—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 20344008HCID 20344008—

Reaction Steps

A mixture of 2.8 g of 4-ethoxycarbonyl-4-(2-phenylthiophenyl)piperidine, free base of Example 17, 1.2 g of allyl bromide, 2.5 g of sodium bicarbonate and a crystal of potassium iodide in 30 ml of dimethylformamide is stirred at 70°-80° C. for 16 hours. Thereafter, the mixture is diluted with water and ether, and the ether layer is separated and then dried. The ether is removed in vacuo and the resulting product is purified by passing through an alumina column, eluted with ether. The purified product is converted in ether to its oxalic acid salt. The salt is recrystallized from a methyl alcohol-acetone-ether mixture to provide 1-allyl-4-ethoxycarbonyl-4-(2-phenylthiophenyl)piperidine oxalate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198419
Source datasetuspto-grants-1980_04
ORD IDord-d87dbf3975ff4fbe8dfe5937918a6803
Source noteuspto-grants-1980_04