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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 532892생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/532892

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물Propylphosphonic anhydrideHCID 111923—
반응물3-Methoxy-2-methyl-3-oxopropanoic acidHCID 300693—
반응물2-(2-Iodophenyl)ethanamineHCID 10514616—
용매Ethyl AcetateHCID 8857—
생성물Methyl 3-((2-iodophenethyl)amino)-2-methyl-3-oxopropanoateHCID 8671134378.5%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853203B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-c313aadacd8f46eb9bbfcda15f98a713
출처 메모uspto-grants-2014_10