HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → 2,4-Dichloro-5-Methylthio-6-Thiocyanopyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | 2,4,6-Trichloro-5-methylsulfanyl-pyrimidine | HCID 12225544 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4-Dichloro-5-Methylthio-6-Thiocyanopyrimidine | HCID 13603264 | 92.9% |
Reaction Steps
In a 50-ml four-necked flask equipped with a thermometer, reflux condenser and stirrer, were charged 2.30 g (0.010 mole) of 5-methylthio-2,4,6-trichloropyrimidine and 15 ml of formic acid. While stirring the contents at room temperature, 1.07 g (0.011 mole) of potassium thiocyanate was added. Then, the resulting mixture was heated and was then stirred at 50° C. for 1 hour. After cooling the reaction mixture, it was poured into a great deal of water. The precipitated solid was collected by filtration and dried to obtain 2.34 g of crude crystals (yield: 92.9%). A portion of the crude crystals was recrystallized from ethyl acetate, thereby obtaining a purified product. m.p. 143°-144.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04774335 |
| Source dataset | uspto-grants-1988_09 |
| ORD ID | ord-beb9851e09c449ca850ab15f37199d4f |
| Source note | uspto-grants-1988_09 |