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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Chloro-2-picoline | HCID 87601 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Chloro-6-(piperidin-1-ylmethyl)pyridine | HCID 13388686 | 41% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04526973 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-ab75ff4a0a7a4d478685daa878ed99d9 |
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| Source note | uspto-grants-1985_07 |
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