HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Pentachloropyridine → 2,3,4,5-Tetrachloropyridine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Pentachloropyridine | HCID 16584 | — |
| Edukt | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Edukt | 2-Hydrazinopyridine | HCID 78645 | — |
| Edukt | 2,3,5,6-Tetrachloro-4-hydrazinylpyridine | HCID 12502192 | — |
| Katalysator | Copper Sulfate | HCID 24462 | — |
| Katalysator | Silver(II) oxide | HCID 92152 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2,3,4,5-Tetrachloropyridine | HCID 76051 | — |
Reaktionsschritte
Another method of preparing tetrachloropyridines is taught in Collins et al., J. Chem. Soc. (C) pages 167-174 (1971) wherein pentachloropyridine is reacted with hydrazine hydrate in ethanol and the resulting tetrachloro-4 and/or 2-hydrazinopyridine is oxidized with aqueous copper sulfate or silver oxide in ethanol. This reference also teaches pyrolyzing tetrachloro-4-hydrazinopyridine in sand at 160° C. to yield tetrachloropyridine. In addition, this reference teaches the preparation of 2,3,6-trichloropyridine from the reaction of tetrachloro-4-hydrazinopyridine with cuprous oxide in hot water.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04127575 |
| Quelldatensatz | uspto-grants-1978_11 |
| ORD ID | ord-4c6c63d271f0442288fa304b35f89b8e |
| Quellennotiz | uspto-grants-1978_11 |