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Boron trifluoride etherate → Benzyl 4-methyl-5-oxo-2-phenyl-1,3-oxazolidine-3-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Boron trifluoride etherate | HCID 8000 | — |
| 反応物 | Benzaldehyde dimethyl acetal | HCID 62375 | — |
| 反応物 | N-(Benzyloxycarbonyl)-DL-alanine | HCID 95657 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | Benzyl 4-methyl-5-oxo-2-phenyl-1,3-oxazolidine-3-carboxylate | HCID 53400837 | — |
反応手順
Boron trifluoride diethyl etherate (12.56 mL, 100 mmol) was added to a −78° C. solution of N-carbobenzoxy-dl-alanine (4.47 g, 20 mmol) and benzaldehyde dimethyl acetal (2.97 mL, 19.8 mmol) in diethyl ether (100 mL). After stirring at ambient temperature for 4 days, the reaction mixture was recooled to 0° C., quenched with saturated aqueous sodium bicarbonate and extracted with diethyl ether. The combined organic extracts were dried (sodium sulfate) and concentrated in vacuo. Chromatography over silica eluting with 5-45% ethyl acetate/hexane afforded benzyl 4-methyl-5-oxo-2-phenyl-1,3-oxazolidine-3-carboxylate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08106070B2 |
| 出典データセット | uspto-grants-2012_01 |
| ORD ID | ord-1c0a8ef29fcd4dfabbecaa38303f60b4 |
| 出典メモ | uspto-grants-2012_01 |