HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,3-Dichloro-5-(trichloromethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | 3-Bromo-2-chloro-5-methylpyridine | HCID 285437 | — |
| Product | 2,3-Dichloro-5-(trichloromethyl)pyridine | HCID 94647 | — |
Reaction Steps
The product from (b) (64 g) in dry carbon tetrachloride (650 ml) was treated with dry hydrogen chloride. The precipitate was broken up and the suspension heated under reflux while dry chlorine was bubbled into the mixture, with illumination from an ultra-violet light source. After 41/2 hours, the mixture was cooled, filtered, and the filtrate evaporated to give the required 2,3-dichloro-5-trichloromethylpyridine. The mass spectrum was consistent with the structure assigned to this compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04508907 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-c851872e2a014f36b16bb292dca03e9e |
| Source note | uspto-grants-1985_04 |