HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042361Generated: November 1, 2026
Hexamethylenetetramine → 6-Bromo-2-Pyridinemethanamine
https://huagongshe.com/reaction/1042361
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Bromo-6-(bromomethyl)pyridine | HCID 12954796 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-Bromo-2-Pyridinemethanamine | HCID 18771861 | — |
Reaction Steps
2-Bromo-6-bromomethyl-pyridine (2.67 g, 10.63 mmol) was combined with hexamethylenetetramine (3.00 g, 21.30 mmol) in chloroform (50 ml) and the resulting reaction mixture was stirred at reflux for 14 hours. The reaction mixture was then cooled to room temperature and the white solid was collected by filtration. The white solid was suspended in ethanol (50 ml) and concentrated HCl (12 ml) was added. The resulting reaction mixture was stirred at 90° C. for 14 hours. Adjustment of pH to 12 was done by the addition of aq 5N NaOH. The reaction mixture was extracted with dichloromethane several times. The combined organic layers were concentrated to yield the title compound. Spectroscopic data: 1H NMR (300 MHz, CDCl3) δ 3.95 (s, 2H) 7.19-7.28 (m, 2H) 7.62 (t, J=7.82 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557853B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-7e4040e942874d17a44cc10771265da1 |
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| Source note | uspto-grants-2013_10 |
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