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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381011Generated: November 4, 2026

Hydrogen Bromide → 4-(5-Bromo-3-methyl-2-pyridinyl)butylamine

https://huagongshe.com/reaction/1381011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13094269HCID 13094269—
ReactantSodium NitriteHCID 23668193—
CatalystCopperHCID 23978—
SolventHydrogen SulfideHCID 402—
SolventWaterHCID 962—
Product4-(5-Bromo-3-methyl-2-pyridinyl)butylamineHCID 13094272—

Reaction Steps

5-Amino-2-(4-aminobutyl)-3-methylpyridine (5.11 g) in hydrobromic acid (48%, 47 ml) was reacted with cuprous bromide (4.98 g) and copper bronze (0.18 g). A solution of sodium nitrite (2.45 g) in water (16 ml) was added at 5° to 8° C. over 45 minutes, the reaction mixture was allowed to stir at 5° to 8° C. for a further hour and then stirred at room temperature for 3.5 hours. The reaction mixture was diluted with water, and hydrogen sulphide gas was passed, while the pH was progressively raised to 11 by the addition of sodium hydroxide solution. The precipitated copper salts were filtered off at intervals during the above procedure. The product was then extracted at pH 11 with chloroform to give 5-bromo-2-(4-aminobutyl)-3-methylpyridine (4.95 g) m.p. 35°-37° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04584381
Source datasetuspto-grants-1986_04
ORD IDord-9c99795000334c9fa3f738471816c878
Source noteuspto-grants-1986_04