HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Diclomezine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 6-(3,5-dichloro-4-methylphenyl)-4-methylthio-4,5-dihydro-3(2H)-pyridazinone | HCID 13367749 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | Diclomezine | HCID 93341 | 94.1% |
Reaction Steps
A suspension of 1.52 g (0.005 mole) of 6-(3,5-dichloro-4-methylphenyl)-4-methylthio-4,5-dihydro-3(2H)-pyridazinone, prepared as described in Example 1(d), in 30 ml of 1N aqueous sodium hydroxide was refluxed for 1 hour. The reaction mixture was allowed to cool and then acidified by adding concentrated hydrochloric acid, whilst water-cooling. The crystals which precipitated were collected by filtration, thoroughly washed with water and then dried to give 1.2 g (yield 94%) of the desired 6-(3,5-dichloro-4-methylphenyl)-3(2H)pyridazinone, melting at 254°-258° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04603201 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-556e16c54ad84d289d6b1655f75d249c |
| Source note | uspto-grants-1986_07 |