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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (3H-Imidazol-4-ylmethyl)-(3-methoxy-phenyl)-amine | HCID 59728243 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (3H-Imidazol-4-ylmethyl)-(3-methoxy-phenyl)-methyl-amine | HCID 59728031 | 75.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586617B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-7c518e62435f4adfa739e08d309e272c |
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| Source note | uspto-grants-2013_11 |
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