HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112669Generated: October 31, 2026
Bromine → 2-Amino-5-bromo-3-(hydroxymethyl)pyridine
https://huagongshe.com/reaction/2112669
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | (2-Aminopyridin-3-yl)methanol | HCID 11159325 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Amino-5-bromo-3-(hydroxymethyl)pyridine | HCID 10891366 | 75.1% |
Reaction Steps
To a stirred solution of 2-amino-3-(hydroxymethyl)pyridine (15.0 g, 121 mmole) in HOAc (300 mL) at RT was added bromine (6.2 mL, 121 mmole) dropwise over 1 hr. A suspension formed after approximately 15 min. After the addition, the reaction was stirred for an additional 1 hr, then was concentrated under vacuum. The residue was taken up in 1.0 M Na2CO3 (500 mL), and the solution was extracted with ethyl acetate (2×250 mL). The combined organic layers were washed with brine, dried (Na2SO4), and concentrated to dryness. The resulting residue was triturated with a small volume of petroleum ether, filtered and dried under vacuum to give the title compound (18.45 g, 75%) as a beige solid: LCMS (ES) m/e 203.2 (M+H)+; 1H NMR (400 MHz, DMSO-d$) δ 7.89 (d, J=2.3 Hz, 1H), 7.52 (s, 1H), 5.92 (br s, 2H), 5.29 (br s, 1H), 4.30 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524843B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-e800355937f341fbba6262b8a70ee9e0 |
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| Source note | uspto-grants-2009_04 |
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