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p-Toluenesulfonic acid → Pyrrolidine, 1-(6-chloro-3,4-dihydro-2-naphthalenyl)-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Pyrrolidine | HCID 31268 | — |
| 反応物 | 6-Chloro-2-tetralone | HCID 4456139 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Pyrrolidine, 1-(6-chloro-3,4-dihydro-2-naphthalenyl)- | HCID 10444008 | — |
反応手順
1155 g (6.4 mol) of 6-chloro-3,4-dihydro-2(1H)-naphthalenone were dissolved in 5 l of toluene, 500 g (7.0 mol) of pyrrolidine and subsequently a solution of 26 g (0.14 mol) of p-toluenesulphonic acid in toluene were added dropwise thereto and the mixture was boiled under reflux. When about 120 ml of water had separated, 4 l of toluene were distilled off and the mixture was left to cool slowly. A solid crystallized out. Filtration and washing with acetone gave 1-(6-chloro-3,4-dihydro-2-naphthyl)pyrrolidine of melting point 117°-118°. Concentration of the mother liquor, suspension of the residue in ether, filtration and washing with acetone gave a further portion of the above product of melting point 117°-118°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04749791 |
| 出典データセット | uspto-grants-1988_06 |
| ORD ID | ord-9f02db5146114d8b94e41f4ce3ed4995 |
| 出典メモ | uspto-grants-1988_06 |