化工社化工社 化学情報印刷レポート · 研究参考用
Tetrahydrofuran → trans-2-(4-Hydroxycyclohexyl)-isoindole-1,3-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | N-Carbethoxyphthalimide | HCID 31187 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | (1s,4s)-4-Aminocyclohexan-1-ol hydrochloride | HCID 522619 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | trans-2-(4-Hydroxycyclohexyl)-isoindole-1,3-dione | HCID 288726 | 72.4% |
反応手順
A solution of 4-aminocyclohexanol hydrochloride (6.08 g, 0.04 mole) in water (60 ml) was brought to pH 8 with aqueous sodium bicarbonate solution. N-carbethoxy-phthalimide (8.76 g, 0.04 mole) was added followed by tetrahydrofuran (until homogenous solution was obtained). The clear solution was stirred at room temperature overnight. During this time a white solid was precipitated. The tetrahydrofuran was removed in vacuo and the remaining aqueous solution was extracted with ethyl acetate until the solution was clear. The ethyl acetate extracts were combined, washed with water, dried (MgSO4) and concentrated to give 4-phthalimido cyclohexanol as a white solid (7.1 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05464864 |
| 出典データセット | uspto-grants-1995_11 |
| ORD ID | ord-8ec7e128fb84498fa001bb7b74ba420b |
| 出典メモ | uspto-grants-1995_11 |