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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18212Generated: October 30, 2026

Bromine → 2-Amino-5-bromo-3-(hydroxymethyl)pyridine hydrobromide

https://huagongshe.com/reaction/18212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant(2-Aminopyridin-3-yl)methanolHCID 11159325—
SolventAcetic AcidHCID 176—
Product2-Amino-5-bromo-3-(hydroxymethyl)pyridine hydrobromideHCID 44119611161.9%

Reaction Steps

To a stirred solution of 2-amino-3-(hydroxymethyl)pyridine (156 g, 1.257 mole) in HOAc (2.5 L) at ambient temperature was added bromine (64.1 mL, 1.257 mole) dropwise over 1 hr. A suspension began to form during the addition. An exotherm to 36° C. was controlled with an ice bath. After the addition, the reaction mixture was stirred at ambient temperature overnight. The yellow precipitate was filtered, washed with ether and air-dried to give the title compound (289 g, 81%): MS (ES) m/e 203.2 (M+H)+; 1H NMR (400 MHz, DMSO-d6, free base) δ 7.89 (d, J=2.3 Hz, 1 H), 7.52 (s, 1 H), 5.92 (br s, 2 H), 5.29 (br s, 1 H), 4.30 (s, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741339B2
Source datasetuspto-grants-2010_06
ORD IDord-267a9d3b52c041c3acd74cd684d5634a
Source noteuspto-grants-2010_06