HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide dimethyl acetal → 4-Methyl-2-(methylsulfanyl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Mercapto-4-methylpyrimidine hydrochloride | HCID 178428687 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Methyl-2-(methylsulfanyl)pyrimidine | HCID 821261 | 84.6% |
Reaction Steps
To 2-mercapto-4-methylpyrimidine·HCl (50.0 g, 0.307 mole) in toluene (750 mL), under argon, was added diisopropylethylamine (80.0 mL, 0.461 mole) followed by N,N-dimethylformamide dimethyl acetal (100 mL) and the mixture heated to reflux for 4 hours. Upon cooling, the reaction was concentrated in vacuo to an oil, dissolved in ether (400 mL), and washed with water (2×50 mL). The organic extract was dried over anhydrous sodium sulfate, filtered and concentrated to an oil which was vacuum distilled to give 2-methylthio-4-methylpyrimidine (36.4 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05859041 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-a19ceaf028184881a3776d4a7655c208 |
| Source note | uspto-grants-1999_01 |