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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437382Generated: October 25, 2026

Sodium Iodide → HCID 13239620, compound

https://huagongshe.com/reaction/437382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant4-ChlorobutyrophenoneHCID 253533—
Reactantrel-(2R,6S)-2,6-DimethylpiperidineHCID 641768—
ProductHCID 13239620HCID 13239620—

Reaction Steps

A mixture of 619 g. of γ-Chlorobutyrophenone, ethylene ketal, 700 g. of cis-2,6-dimethylpiperidine and 16 g. of sodium iodide is stirred and heated at reflux for 48 hours. The mixture is cooled, diluted with 1 l. of anhydrous ether and filtered to remove cis-2,6-dimethylpiperidine hydrochloride. The filter cake is washed with 1 l. of ether and the filtrate and washings combined. The resulting ether solution is washed five times with 500 ml. portions of water, then extracted with a solution of 300 ml. of concentrated hydrochloric acid in 3 l. of water. The acid extract is washed with 500 ml. of ether, then heated to 70°-80° and allowed to cool to room temperature over a period of 16 hours. The resulting solution is basified with 50% aqueous sodium hydroxide and the organic layer is separated. The aqueous layer is extracted with 500 ml. of ether and the extract is combined with the organic layer. The combined extract is washed several times with water, dried and evaporated. The oily residue is distilled at reduced pressure to give cis-γ-(2,6-dimethylpiperidino)butyrophenone; b.p. 138°-141° C./0.1 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031101
Source datasetuspto-grants-1977_06
ORD IDord-cf952834d21840f5b0184b6f2c8b8296
Source noteuspto-grants-1977_06