関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Naphthol | HCID 7005 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 1-(Iso-propyl)-3-benzyloxyazetidine | HCID 20517324 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 1-(alpha-Naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propane | HCID 13055708 | 79% |
反応手順
To a mixture of 6.2 parts of 1-(iso-propyl)-3-benzyloxyazetidine and 43 parts of α-naphthol 1.5 parts of sodium hydroxide was added, and the mixture was heated at 200° C. for 16 hours. The reaction mixture was cooled, and 100 parts of ether were added thereto. Excessive α-naphthol was removed by extraction with 2N-sodium hydroxide aqueous solution. The remaining ether layr was washed in water and dried over anhydrous sodium sulfate. After distillation of ether, the residue was subjected to distillation to yield 8.3 parts of 1-(α-naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propane boiling at 192°-195° C. The yield was 79%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04018824 |
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| 出典データセット | uspto-grants-1977_04 |
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| ORD ID | ord-08d8eafb95d447d1a0a5fec4a5d9df11 |
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| 出典メモ | uspto-grants-1977_04 |
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