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HRID 532892作成日:2026年10月27日

Triethylamine → Methyl 3-((2-iodophenethyl)amino)-2-methyl-3-oxopropanoate

https://huagongshe.com/reaction/532892

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物Propylphosphonic anhydrideHCID 111923—
反応物3-Methoxy-2-methyl-3-oxopropanoic acidHCID 300693—
反応物2-(2-Iodophenyl)ethanamineHCID 10514616—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 3-((2-iodophenethyl)amino)-2-methyl-3-oxopropanoateHCID 8671134378.5%

反応手順

A solution of T3P in AcOEt (50%, 26.2 mL, 44.0 mmol) was added dropwise at 0° C. under N2 to a clear solution of 2-(2-iodophenyl)ethanamine (9.45 g, 38.2 mmol), 3-methoxy-2-methyl-3-oxopropanoic acid (5.05 g, 38.2 mmol) and Et3N (10.7 mL, 76.0 mmol) in AcOEt (350 mL). The mixture was stirred at RT for 6 days. A 2N aqueous solution of NaOH (50 mL) was then added to the reaction and the mixture was extracted with AcOEt. The combined org. layers were then dried over Na2SO4, filtered and concentrated in vacuo. The yellow oil obtained was purified by flash chromatography (SiO2, cHEx/AcOEt 100:0 to 50:50) to afford the title compound (10.83 g) as a clear oil. UPLC-MS: MS 362.2 (M+H+); UPLC rt 0.95 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853203B2
出典データセットuspto-grants-2014_10
ORD IDord-c313aadacd8f46eb9bbfcda15f98a713
出典メモuspto-grants-2014_10