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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245183Generated: October 26, 2026

2-(Methylamino)ethanol → 2-(Methyl-[2,2';6'2'']terpyridine-4'yl-amino)-ethanol

https://huagongshe.com/reaction/2245183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methylamino)ethanolHCID 8016—
Reactant4'-Chloro-2,2';6,2''-terpyridineHCID 15861407—
CatalystZincchlorideHCID 3007855—
Solvent2-Methyl-2-butanolHCID 6405—
Product2-(Methyl-[2,2';6'2'']terpyridine-4'yl-amino)-ethanolHCID 1049487084.5%

Reaction Steps

129 g (1.72 mol) 2-methylamino-ethanol and 390 mg (2.86 mmol) zinc(II)-chloride are successively added to a suspension of 15.3 g (57.2 mmol) 4′-chloro-2,2′;6,2″-terpyridine in 100 ml 2-methyl-2-butanol. The reaction mixture is refluxed for 2.5 days. A brown suspension is obtained, which is evaporated under vacuum to a yellow-brown solid product. 100 ml water is added to this product and stirred at room temperature for 20 minutes. Then, the obtained mixture is filtrated and the filter residue dried for 12 hours at (45° C., 10 mbar). 14.8 g (84%) of 2-(methyl-[2,2′;6′2″]terpyridine-4′yl-amino)-ethanol as colourless solid product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07682404B2
Source datasetuspto-grants-2010_03
ORD IDord-d059e1d43ad049189646d43be0908f26
Source noteuspto-grants-2010_03