HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 6-Methyl-2-Trichloromethyl-4-Pyrimidinyl Diethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178429333 | HCID 178429333 | — |
| Product | 6-Methyl-2-Trichloromethyl-4-Pyrimidinyl Diethylcarbamate | HCID 13041532 | — |
Reaction Steps
A mixture of 5.8 g (0.027 mole) 4-hydroxy-6-methyl-2-trichloromethylpyrimidine, 3.3 g (0.024 mole) potassium carbonate, 3.3 g (0.024 mole) dimethylcarbamoyl chloride, and 100 ml acetone was refluxed 5 hours. A precipitate was filtered out and the filtrate rotary evaporated to give 10.2 g residue. This was taken up in chloroform, the solution washed with 1% sodium hydroxide, water, and dried over anhydrous magnesium sulfate. Rotary evaporation yielded 5.2 g residue which was recrystallized from petroleum ether to give 2.1 g (24% yield) of product. An analytical sample recrystallized a second time from petroleum ether had mp 77°-77.5° C. The structure was confirmed via infrared and elemental analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04343803 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-e649a692c4fb41879d7c7deb50b8f5d0 |
| Source note | uspto-grants-1982_08 |