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Phosphorus sulfide (P2S5) → 6-(3,5-Dichloro-4-methylphenyl)-3(2H)pyridazinethione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| 反応物 | Diclomezine | HCID 93341 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 6-(3,5-Dichloro-4-methylphenyl)-3(2H)pyridazinethione | HCID 12945891 | 56% |
反応手順
12.75 g of 6-(3,5-dichloro-4-methylphenyl)-3-pyridazone and 22 g of phosphorus pentasulphide in 80 ml of pyridine were heated under reflux on an oil bath for 7 hours. The reaction mixture was then cooled to room temperature and its volume was reduced by one-half by distilling off the pyridine under reduced pressure. 300 ml of ethyl acetate were added to the residue and the mixture was poured into ice-water. After stirring the mixture for a short time, the resulting yellow solid was collected by filtration, washed with water and dried to give 7.5 g (56%) of the desired compound. After recrystallizing the compound from a 10:1 by volume mixture of ethanol and dioxan, the compound melted at 255°-258° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04279908 |
| 出典データセット | uspto-grants-1981_07 |
| ORD ID | ord-2dc26b45efdb4f6d8321322acc64cfb9 |
| 出典メモ | uspto-grants-1981_07 |