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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043347Generated: November 1, 2026

Hydrochloric Acid → (3H-Imidazol-4-ylmethyl)-(3-methoxy-phenyl)-methyl-amine

https://huagongshe.com/reaction/2043347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(3H-Imidazol-4-ylmethyl)-(3-methoxy-phenyl)-amineHCID 59728243—
SolventAcetonitrileHCID 6342—
Product(3H-Imidazol-4-ylmethyl)-(3-methoxy-phenyl)-methyl-amineHCID 5972803175.8%

Reaction Steps

(3H-Imidazol-4-ylmethyl)-(3-methoxy-phenyl)-amine (0.070 g, 0.34 mmol) was dissolved in acetonitrile (10 ml). Then formaldehyde (0.0.06 ml, 0.86 mmol, 37% aqueous solution) and sodium cyanoborohydride (0.065 g, 1.03 mmol) were added and the reaction mixture was allowed to stir at room temperature for 10 minutes. The reaction mixture was then acidified to pH 2-3 by dropwise addition of concentrated hydrochloric acid whereupon precipitation occurred. The mixture was stirred for a further 1 h at room temperature before being concentrated in vacuo. The residue was taken up in ethyl acetate, washed with 1 M aqueous sodium hydroxide solution and the organic layer was dried over magnesium sulfate and concentrated in vacuo. The residue was purified using flash chromatography (column: Isolute® Flash-NH2 from Separtis; eluent: methanol/dichloromethane gradient) to yield a white solid (0.056 g, 75%); MS (ISP): 218.3 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586617B2
Source datasetuspto-grants-2013_11
ORD IDord-7c518e62435f4adfa739e08d309e272c
Source noteuspto-grants-2013_11