HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741791Generated: October 25, 2026
Chlorobenzene → 2,6-Dichloro-3-methylpyridine
https://huagongshe.com/reaction/1741791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-5-methylpyridin-1-ium-1-olate | HCID 13431623 | — |
| Product | 2,6-Dichloro-3-methylpyridine | HCID 817088 | — |
Reaction Steps
101.5 g (0.50 mol) of o-phthaloyl chloride in 50 ml of chlorobenzene are added dropwise under nitrogen to a solution of 35.9 g (0.25 mol) of 2-chloro-5-methylpyridine-1-oxide and 50.6 g (0.50 mol) of triethylamine in 200 ml of chlorobenzene in the course of 30 min. The mixture is subsequently heated under reflux for a further 12 hours, then the precipitate is filtered off with suction, the filter cake is washed with 50 ml of methylene chloride and the solvent is removed by distillation. The bottom is subjected to steam distillation, the pH of 6 being maintained by continuously adding 45 per cent sodium hydroxide solution. The distillate is extracted three times using 100 ml of methylene chloride each time, the solvent is removed by distillation and the residue is recrystallized from hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05334724 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-76f7ac663a924419820cbce056b736ef |
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| Source note | uspto-grants-1994_08 |
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