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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396149Generated: October 31, 2026

Sodium Chloride → HCID 18988032, compound

https://huagongshe.com/reaction/2396149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl [2-(pyridin-2-yl)ethyl]carbamateHCID 22027815—
SolventDimethylformamideHCID 6228—
ProductHCID 18988032HCID 1898803276.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-[2-(N-t-butoxycarbonylamino)ethyl]-pyridine (1.8 g) in N,N-dimethylformamide (7 ml) was added dropwise to a suspension of sodium hydride (0.39 g) in N,N-dimethylformamide (7 ml) which was cooled at 0° C. The mixture was stirred at 0° C. for 1 hour. Methyl iodide (1.4 g) was added to this solution at the same temperature. After stirring at 0° C. for 1 hour and at ambient temperature for 2 hours, the mixture was poured into ice water, saturated with sodium chloride, and extracted with ethyl acetate 3 times. The combined organic layer was washed with saturated sodium thiosulfate, saturated sodium bicarbonate and saturated sodium chloride successively, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified with silica gel chromatography (ethyl acetate:n-hexane, 3:1, V/V, as eluent) to give 2-[2-(N-t-butoxycarbonyl-N-methylamino)ethyl]-pyridine (1.47 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05491132
Source datasetuspto-grants-1996_02
ORD IDord-28459f0e9bde4a6fa0552dfc1c51ed2d
Source noteuspto-grants-1996_02