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m-Chloroperbenzoic acid → 1-Methyl-4-phenoxy-4-phenylpiperidine N-oxide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | m-Chloroperbenzoic acid | HCID 70297 | — |
| 反応物 | Piperidine, 1-methyl-4-phenoxy-4-phenyl- | HCID 3060394 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-Methyl-4-phenoxy-4-phenylpiperidine N-oxide | HCID 53888329 | — |
反応手順
1.5 g of 1-methyl-4-phenoxy-4-phenylpiperidine are dissolved in 4 ml of methanol, and 1.7 g of 80% strength m-chloroperbenzoic acid, dissolved in methanol, are added slowly thereto while cooling with ice. After stirring the mixture at room temperature for 3 hours, the solvent is stripped off and the residue is partitioned between concentrated sodium hydroxide solution and chloroform. The crude N-oxide hydrate (which remains after drying the chloroform phase and evaporating off the solvent) is taken up in a little methanol, and the equivalent amount of methanolic fumaric acid is added. 1 g of a colorless precipitate is obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04333942 |
| 出典データセット | uspto-grants-1982_06 |
| ORD ID | ord-73c031d5a4e942119bc30554cd4ce55d |
| 出典メモ | uspto-grants-1982_06 |