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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409624Generated: October 31, 2026

1-Methylimidazole → HCID 86680637, compound

https://huagongshe.com/reaction/409624

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantTetrahydrofuranHCID 8028—
ReactantBromodiphenylmethaneHCID 236603—
Reactant2-(pyridin-2-ylamino)ethanolHCID 420844—
ProductHCID 86680637HCID 8668063762%

Reaction Steps

Diphenylmethyl bromide (0.1 mol; 24.75 g) was dissolved in 25 ml of tetrahydrofuran and placed in a flask together with N-pyridylethanolamine (0.05 mole-6.9 g) and 0.5 ml of catalytic N-methylimidazol, and then left for 72 hours in a dryer at temperature of 65° C. The product of this reaction was purified on a column filled with silica gel 60 of a particle size 70-230 mesh. Methanol gradient in methylene chloride was used as an eluting phase. Then the fractions containing the product of the reaction (N-pyridyl-N-[diphenylmethyl]aminoethanol) were isolated and combined. The excess of solvent was evaporated. The compound was characterized by means of the 1HNMR and 13CNMR spectra, presented in FIG. 9. 19.03 g were obtained (a yield of 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759509B2
Source datasetuspto-grants-2014_06
ORD IDord-567c8ac76e724cb2a89b253a585c5d1f
Source noteuspto-grants-2014_06