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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902530Generated: November 2, 2026

Methyl iodide → HCID 20515681, compound

https://huagongshe.com/reaction/1902530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-MethylindoleHCID 7224—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(Chloromethyl)pyridinium chlorideHCID 74570—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 20515681HCID 20515681—

Reaction Steps

Methyl iodide (32.0 g) in dry ether (100 ml) was added dropwise to a stirred mixture of magnesium and dry ether (50 ml) at such a rate that the reaction was not too vigorous. After completion of the addition the mixture was heated under reflux for 30 minutes and then cooled to 0°. A solution of 2-methylindole (16.9 g) in dry ether (100 ml) was added dropwise with stirring and the resulting mixture was then heated under reflux for 1.5 hours. It was then cooled to 0° and 4-chloromethyl pyridine hydrochloride (10.5 g) was added portionwise with stirring. The mixture was heated under reflux with stirring for 3 hours and then cooled. A solution of ammonium chloride (30 g) in water (200 ml) was added dropwise with stirring and then the layers were separated. The ether layer was dried (Na2SO4) and evaporated to give an oil which was chromatographed on silica gel. Elution with chloroform initially gave some impurity together with the starting indole. Further elution gave 2-methyl-3-(4-pyridylmethyl)indole (8.0 g), m.p. 126°-127° C. (from ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04363912
Source datasetuspto-grants-1982_12
ORD IDord-162644b01e46495d89f6a5ab4be622dc
Source noteuspto-grants-1982_12