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Acetone → O-[2-(2,6-dimethyl-3-pyridylamino)-2-ketoethyl] O-methyl O-(4-chlorophenyl) phosphate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetone | HCID 180 | — |
| 反応物 | N-(2,6-dimethyl-3-pyridyl)-alpha-chloroacetamide | HCID 21493317 | — |
| 反応物 | potassium O-methyl O-(4-chlorophenyl) phosphate | HCID 68134157 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | O-[2-(2,6-dimethyl-3-pyridylamino)-2-ketoethyl] O-methyl O-(4-chlorophenyl) phosphate | HCID 54372328 | — |
反応手順
N-(2,6-Dimethyl-3-pyridyl)-α-chloroacetamide (32.2 grams), potassium O-methyl O-(4-chlorophenyl) phosphate (26 grams) and acetone (200 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at reflux for a period of about 24 hours. After this time the mixture is stripped of solvent on a steam bath and the resulting residue is dissolved in ether. The ether solution is washed with water and is dried over magnesium sulfate. The dried solution is then evaporated under vacuum to yield the desired product O-[2-(2,6-dimethyl-3-pyridylamino)-2-ketoethyl] O-methyl O-(4-chlorophenyl) phosphate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03996352 |
| 出典データセット | uspto-grants-1976_12 |
| ORD ID | ord-9a4d6d8b58a642e29525e9cf6126711e |
| 出典メモ | uspto-grants-1976_12 |