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Tetrahydrofuran → N-{3-hydroxybicyclo[1.1.1]pentan-1-yl}acetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 3-Acetamidobicyclo[1.1.1]pentan-1-yl acetate | HCID 86287955 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | N-{3-hydroxybicyclo[1.1.1]pentan-1-yl}acetamide | HCID 86287953 | — |
反応手順
To a THF (2 mL) solution of 3-acetamidobicyclo[1.1.1]pentan-1-yl acetate (3) (1 mmol) is added methanol (0.7 mL) followed by a aqueous solution of NaOH (1.4 M, 0.7 mL, 1 eq) at room temperature. The mixture is stirred and monitored by TLC. After complete consumption of the starting material, saturated ammonium chloride is added and the mixture is stirred for 5 min. The volatiles are removed under vacuum and the resultant mixture is extracted with EtOAc (3×). The organic layers are combined, dried (magnesium sulfate), filtered, and concentrated. The crude residue is subjected to flash chromatography (silica gel, EtOAc/hexanes) to give N-(3-hydroxybicyclo[1.1.1]pentan-1-yl)acetamide (1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09447025B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-e3a6ee10a94843b489eb9be554bfc059 |
| 出典メモ | uspto-grants-2016_09 |