HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2,4,6-Trimethoxy-5-(methylsulfanyl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Chloro-2,6-dimethoxy-5-(methylsulfanyl)pyrimidine | HCID 15590370 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4,6-Trimethoxy-5-(methylsulfanyl)pyrimidine | HCID 15590371 | — |
Reaction Steps
Charged into a 100-milliliter, 4-necked flask equipped with a reflux condenser, thermometer and stirrer were 2.2 g of 6-chloro-2,4-dimethoxy-5-methylthiopyrimidine and 40 ml of methanol. They were stirred into a homogeneous solution. Subsequent to an addition of 2.0 g of potassium hydroxide, the resultant mixture was heated and refluxed, with thorough stirring, for 3 hours. The liquid reaction mixture was then poured into water and the resultant solid precipitate was collected by filtration. It was recrystallized from isopropyl alcohol, thereby obtaining 5-methylthio-2,4,6-trimethoxypyrimidine (m.p. 90°-91° C.). Yield: 1.96 g(90.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04540698 |
| Source dataset | uspto-grants-1985_09 |
| ORD ID | ord-5200ee52dbcb4c3fbcb2c98c0c89c2c2 |
| Source note | uspto-grants-1985_09 |