HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 6-Chloro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Chloro-3-(4-hydroxyphenoxy)-2-pyrazinecarbonitrile | HCID 22662769 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Chloro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrile | HCID 22662848 | 101.7% |
Reaction Steps
In 8 mL of dimethylformamide was dissolved 0.4 g of 6-chloro-3-(4-hydroxyphenoxy)-2-pyrazinecarbonitrile. After adding 0.5 ml of iodomethane and 0.89 g of potassium carbonate, the mixture thus obtained was stirred at room temperature for 30 minutes. The reaction mixture was added to a mixture of 10 mL of ethyl acetate and 30 mL of water, and the organic layer was separated. The organic layer was washed successively with water and saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. Thus, 0.43 g of 6-chloro-3-(4-methoxyphenoxy)-2-pyrazinecarbonitrile was obtained as a yellow-brown colored solid product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06800629B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-d77dcb9fa0ed4b6d8870503764a58ad8 |
| Source note | uspto-grants-2004_10 |