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Hydrochloric Acid → benzyl 4-[(2RS)-4-oxoazetidin-2-yl]but-2-enoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | benzyl 4-[(2RS)-1-(tert-butyldimethylsilyl)-4-oxoazetidin-2-yl]but-2-enoate | HCID 53904921 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | benzyl 4-[(2RS)-4-oxoazetidin-2-yl]but-2-enoate | HCID 53759236 | 97.7% |
反応手順
To a solution of benzyl 4-[(2RS)-1-(tert-butyldimethylsilyl)-4-oxoazetidin-2-yl]but-2-enoate (45 mg) in methanol was added 1 N hydrochloric acid (0.1 ml) at 0°. After stirring at room temperature for 2.5 hours, the reaction mixture was neutrallized to pH 7 with saturated aqueous sodium bicarbonate. The resultant solution was concentrated, taken up into ethyl acetate (15 ml), and washed in turn with water and brine. Drying over magnesium sulfate and removal of the solvent left an oil, which was chromatographed on a silica gel plate (developing solvent: 6% methanol in dichloromethane) to give benzyl 4-[(2RS)-4-oxoazetidin-2-yl]but-2-enoate (30 mg) as a crystalline solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04383945 |
| 出典データセット | uspto-grants-1983_05 |
| ORD ID | ord-966800ca7b2d4e40ad476f1b342a8c9c |
| 出典メモ | uspto-grants-1983_05 |