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p-Toluenesulfonic acid → 2-(2-Buten-1-yl)-8-methoxy-1-tetralone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 2,2-Dimethoxypropane | HCID 6495 | — |
| 反応物 | 3-Buten-2-ol | HCID 11716 | — |
| 反応物 | 8-Methoxy-3,4-dihydronaphthalen-1(2H)-one | HCID 11275335 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2-(2-Buten-1-yl)-8-methoxy-1-tetralone | HCID 54124897 | 22% |
反応手順
13.7 g of 8-methoxy-1-tetralone were dissolved in 140 ml of toluene under argon and added to 13.3 ml of 3-buten-2-ol, 14.2 ml of 2,2-dimethoxypropane and 300 mg of p-toluenesulfonic acid. The reaction solution was heated to reflux for 90 hours. The solvent was removed in a vacuum and the residue was chromatographed on 500 g of silica gel firstly with hexane/ethyl acetate 9:1, then with hexane/ethyl acetate 4:1 and finally with hexane/ethyl acetate 1:1. In addition to large amounts of unreacted educt (8.3 g) there were obtained 3.95 g (22%) of 2-(2-buten-1-yl)-8-methoxy-1-tetralone as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05646173 |
| 出典データセット | uspto-grants-1997_07 |
| ORD ID | ord-2e1fc451f6ab48748f84d89860dd7c53 |
| 出典メモ | uspto-grants-1997_07 |