Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701107Generated: November 2, 2026

Potassium Iodide → 1-Benzyl-2,6-diethyl-2,3,6-trimethyl-4-benzamidopiperidine

https://huagongshe.com/reaction/1701107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(2,6-Diethyl-2,3,6-trimethylpiperidin-4-yl)benzamideHCID 22486017—
SolventTolueneHCID 1140—
SolventSulfolaneHCID 31347—
Product1-Benzyl-2,6-diethyl-2,3,6-trimethyl-4-benzamidopiperidineHCID 20348330—

Reaction Steps

20 g of 2,6-diethyl-2,3,6-trimethyl-4-benzamidopiperidine (compound no. 9), 12.5 g of benzylbromide, 1 g of potassium iodide and 20 g of potassium carbonate are stirred in 200 ml of tetrahydrothiophene dioxide (sulpholane) at 110° C. for 4 days. Thereafter the reaction mixture is diluted with 200 ml of toluene, cooled to room temperature and purified by filtration. The filtrate is washed four times with about 200 ml of water, the toluene phase is dried over sodium sulfate and evaporated under vacuum. Crystallization of the residue from acetic acid ethyl ester yields 1-benzyl-2,6-diethyl-2,3,6-trimethyl-4-benzamidopiperidine (compound no. 48); m.p. 234°-236° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04191683
Source datasetuspto-grants-1980_03
ORD IDord-b3576292e75e412ab03c0bf3c6f01fdc
Source noteuspto-grants-1980_03