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Benzyl acetone → 5-[1-Hydroxy-2-(1-methyl-3-phenylpropyl)aminoethyl]-o-anisamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl acetone | HCID 17355 | — |
| 反応物 | 5-(2-Amino-1-hydroxyethyl)-o-anisamide | HCID 20318583 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Platinum | HCID 23939 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-[1-Hydroxy-2-(1-methyl-3-phenylpropyl)aminoethyl]-o-anisamide | HCID 20318587 | — |
反応手順
To a solution of the above 5-(2-amino-1-hydroxyethyl)-o-anisamide in ethanol (70ml) was added benzyl acetone (1.5g), and the mixture was gently refluxed for 1 hour. The cooled solution was then added to a suspension of pre-reduced 5% platinum on charcoal (0.4g) in ethanol (10 ml) and hydrogenated until uptake was complete. Hydrogen uptake was complete within 14 hours. The catalyst and solvent were removed to leave 5-[1-hydroxy-2-(1-methyl-3-phenylpropyl)aminoethyl]-o-anisamide as an oil (2.36g) which slowly crystallised on rubbing with ether, m.p. 110°-148°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04101579 |
| 出典データセット | uspto-grants-1978_07 |
| ORD ID | ord-2e8c743f4f4c4ba6909a6b3e551855d0 |
| 出典メモ | uspto-grants-1978_07 |