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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272507Generated: November 1, 2026

Hydrogen Bromide → 3,6-Dibromo-2-methylpyridine

https://huagongshe.com/reaction/1272507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
Reactant2-Pyridinamine, 5-bromo-6-methyl-HCID 170678—
ReactantHCID 18457531HCID 18457531—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product3,6-Dibromo-2-methylpyridineHCID 2762946183.1%

Reaction Conditions

Temperature2 °C

Reaction Steps

5-Bromo-2-amino-6-picoline (7.0 kg) and 5-bromo-2-amino-6-picoline hydrobromide (7.0 kg) (based on the starting material analyses, this was equal to 11 kg or 41 mol of starting material) are dissolved into 48% hydrobromic acid (107.0 kg, 635 mol, 15.49 eq) at <35° C. The solution was cooled to 2° C. and bromine (27.3 kg, 171 mol, 4.17 eq) was charged over 45 min at 0–5° C. A solution of sodium nitrite (8.1 kg, 117 mol, 2.86 eq) in 20 L of water was charged over 1.5 hours at −1 to 5° C. The contents were held one hour and the pH was adjusted to 12.5 using 50% aqueous sodium hydroxide (70.0 kg). The contents were warmed to 20° C. over one hour and the solids were collected in a polypropylene bag on a centrifuge. The solids were washed with water (75 L) to produce 12.0 kg of moist 2,5-dibromo-6-picoline, determined to be 83 wgt % product (68% yield). Part of this was dried for the purposes of recording the 13C NMR spectrum: 13C NMR (400 MHz, CDCl3) δ 158.8, 141.9, 139.4, 126.7, 120.6, 24.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208596B2
Source datasetuspto-grants-2007_04
ORD IDord-9d0b41596a37472dbab6c483ebb556ad
Source noteuspto-grants-2007_04