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Ethyl 2-(benzylamino)propanoate → Methyl 4-(benzyl(1-ethoxy-1-oxopropan-2-yl)amino)butanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl 2-(benzylamino)propanoate | HCID 222273 | — |
| 反応物 | 2-Ketobutyric acid methyl ester | HCID 545127 | — |
| 溶媒 | 1,2-Dichloroethane | HCID 11 | — |
| 生成物 | Methyl 4-(benzyl(1-ethoxy-1-oxopropan-2-yl)amino)butanoate | HCID 67423852 | — |
反応手順
2-Benzylamino-propionic acid ethyl ester (1.4 g, 6.7 mmol), methyl oxo-butanoate (1.7 g, 13.5 mmol), TEA (1.9 mL, 13.5 mmol) and NaBH(Oac)3 (2.9 g, 13.5 mmol) are taken up in 1,2-DCE (35 mL) and stirred at rt for 4 h. The reaction is partitioned between DCM and saturated aqueous NaHCO3. The organic layer is removed, dried over anhydrous Na2SO4, and concentrated in vacuo. The crude residue is used without further purification. MS (ESI) m/z 308.3 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08242125B2 |
| 出典データセット | uspto-grants-2012_08 |
| ORD ID | ord-26083ffd694c4664905f8168ed074c81 |
| 出典メモ | uspto-grants-2012_08 |