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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370541Generated: October 26, 2026

Benzoyl Peroxide → 2-Chloro-6-(piperidin-1-ylmethyl)pyridine

https://huagongshe.com/reaction/370541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantPiperidineHCID 8082—
ReactantN-bromobutanimideHCID 67184—
Reactant6-Chloro-2-picolineHCID 87601—
SolventCarbon TetrachlorideHCID 5943—
Product2-Chloro-6-(piperidin-1-ylmethyl)pyridineHCID 1338868641%

Reaction Steps

To 2-chloro-6-methylpyridine (50.0 g, 0.392 mole) in 393 mL of carbon tetrachloride was added N-bromosuccinimide (87.2 g, 0.49 mole) and 1.0 g of benzoyl peroxide. The mixture was stirred at reflux for 22 hours, cooled to 10° and filtered. The chilled filtrate then was treated slowly with piperidine (83.5 g, 0.98 mole) and allowed to stir at ambient temperature for 18 hours. After removal of the piperidine hydrobromide by filtration, the filtrate was concentrated to about half volume and extracted with 6N HCl (65 mL) and 3N HCl (40 mL). The acid extracts were made basic with 40% sodium hydroxide and the product was extracted into methylene chloride. The solvent was evaporated and the residue distilled to yield 41% of the title compound as a colorless oil, b.p. 101°-103°/0.45 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04526973
Source datasetuspto-grants-1985_07
ORD IDord-ab75ff4a0a7a4d478685daa878ed99d9
Source noteuspto-grants-1985_07