HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-tert-butyl-5-chloro-4-methylpyridazin-3-(2H)-one → 2-t-butyl-5-chloro-4-ethyl-3(2H)-pyridazinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-tert-butyl-5-chloro-4-methylpyridazin-3-(2H)-one | HCID 13822264 | — |
| Reactant | HCID 19903158 | HCID 19903158 | — |
| Reactant | 4-n-butyl-5-chloro-2-t-butyl-3(2H)pyridazinone | HCID 21285475 | — |
| Reactant | 4-n-pentyl-5-chloro-2-t-butyl-3(2H)pyridazinone | HCID 21285493 | — |
| Product | 2-t-butyl-5-chloro-4-ethyl-3(2H)-pyridazinone | HCID 13825010 | — |
Reaction Steps
In the same manner as above, the following compounds were prepared from the corresponding 2-alkyl-4,5-dichloro-3(2H)pyridazinones and alkyl magnesium halides: 4-Methyl-5-chloro-2-t-butyl-3(2H) pyridazinone [oily substance, boiling point: 60°-62° C. (0.22 mmHg)], 4-n-propyl-5-chloro-2-t-butyl-3(2H) pyridazinone (oily substance), 4-n-butyl-5-chloro-2-t-butyl-3(2H)pyridazinone (only substance) and 4-n-pentyl-5-chloro-2-t-butyl-3(2H)pyridazinone (oily substance).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04783462 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-a3ffa75dbdd34aa28e977d83e75f4bc0 |
| Source note | uspto-grants-1988_11 |