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HRID 884538作成日:2026年10月25日

Ethyl 2-(benzylamino)propanoate → Methyl 4-(benzyl(1-ethoxy-1-oxopropan-2-yl)amino)butanoate

https://huagongshe.com/reaction/884538

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-(benzylamino)propanoateHCID 222273—
反応物2-Ketobutyric acid methyl esterHCID 545127—
溶媒1,2-DichloroethaneHCID 11—
生成物Methyl 4-(benzyl(1-ethoxy-1-oxopropan-2-yl)amino)butanoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08242125B2
出典データセットuspto-grants-2012_08
ORD IDord-26083ffd694c4664905f8168ed074c81
出典メモuspto-grants-2012_08