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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210942Generated: November 2, 2026

Methyl iodide → 2-[[N-(tert-butyloxycarbonyl)-N-methylamino]methyl]pyridine

https://huagongshe.com/reaction/2210942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantN-Boc-2-aminomethylpyridineHCID 12069550—
SolventTetrahydrofuranHCID 8028—
Product2-[[N-(tert-butyloxycarbonyl)-N-methylamino]methyl]pyridineHCID 1960621370.6%

Reaction Steps

A solution of 19.8 g (95 mmol) of 2-(N-(t-butyloxycarbonyl)aminomethyl)pyridine in anhydrous tetrahydrofuran was cooled under N2 atmosphere to 0° C. and treated with 4.95 g (124 mmol) of sodium hydride (60% dispersion in oil). The solution was stirred for 15 min, treated dropwise with 7.1 ml (114 mmol) of methyl iodide, stirred at ambient temperature for 2 h, and quenched cautiously with water. The resulting mixture was partitioned between ether and water, dried over Na2SO4, and concentrated in vacuo. Chromatography on silica gel provided 14.9 g (70%) of the desired compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05461067
Source datasetuspto-grants-1995_10
ORD IDord-f35371a81db141818b00ca360b708355
Source noteuspto-grants-1995_10