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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21371Generated: October 29, 2026

Methyl iodide → 4-[(Ethylthio)methyl]-1-methyl-1,2,3,6-tetrahydropyridine

https://huagongshe.com/reaction/21371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant4-[(Ethylthio)methyl]pyridineHCID 14442205—
SolventAcetonitrileHCID 6342—
Product4-[(Ethylthio)methyl]-1-methyl-1,2,3,6-tetrahydropyridineHCID 1444221547.6%

Reaction Steps

8.2 g (0.054 mol) of 4-[(ethylthio)methyl]pyridine are dissolved in 60 ml of acetonitrile and then 9.1 g of methyliodide are added. After 12 hours the reaction mixture is evaporated down in vacuo. The residue is reacted analogously to Example 1 b) with sodium borohydride in methanol and worked up. The crude product obtained is distilled (5.2 g; 56.3% of theory; b.p. 118°-120° C./20 mbar) and then chromatographed on neutral aluminium oxide using chloroform as eluant. 4.4 g of 4-[(ethylthio)methyl]-1-methyl-1,2,3,6-tetrahydropyridine are obtained, which is converted with one equivalent of maleic acid into the maleate (m.p. 102°-105° C., from ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05422353
Source datasetuspto-grants-1995_06
ORD IDord-833ce92ccfa44f91b77719638dad4bee
Source noteuspto-grants-1995_06