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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486070Generated: October 30, 2026

Methyl iodide → HCID 15733061, compound

https://huagongshe.com/reaction/486070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant1-Benzyl-3,4-dimethylpyridin-1-ium chlorideHCID 13978617—
SolventDiethyl EtherHCID 3283—
ProductHCID 15733061HCID 1573306188.8%

Reaction Steps

A solution of methyl iodide (112 mL, 1.8 mole) in ether (225 mL) was added dropwise to a suspension of magnesium turnings (44 g, 1.8 mole) in ether (225 mL) under nitrogen over a period of 1 hour. The mixture was stirred at room temperature for 1 hour, transferred into a 1000 mL addition funnel and then was added to a suspension of N-(phenylmethyl)-3,4-dimethylpyridinium chloride (350.7 g, 1.5 mole) in ether (1500 mL) under a nitrogen atmosphere. The reaction mixture was stirred at room temperature for 24 hours and was then poured into a solution of saturated ammonium chloride (3 L). The organic layer was separated and the aqueous layer was extracted with ether (1000 mL). The combined ether layers were washed with water (500 mL), then brine (500 mL) and were dried over sodium sulfate and potassium carbonate. The solvent was removed in vacuo to afford 284.1 g (76%) of 1,2-dihydro-N-(phenylmethyl)-2,3,4-trimethylpyridine as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290796
Source datasetuspto-grants-1994_03
ORD IDord-27e39e3f0eb247b3a0b3b11c1ebaa605
Source noteuspto-grants-1994_03