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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 532892Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/532892

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktSodium HydroxideHCID 14798—
EduktPropylphosphonic anhydrideHCID 111923—
Edukt3-Methoxy-2-methyl-3-oxopropanoic acidHCID 300693—
Edukt2-(2-Iodophenyl)ethanamineHCID 10514616—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 3-((2-iodophenethyl)amino)-2-methyl-3-oxopropanoateHCID 8671134378,5%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08853203B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-c313aadacd8f46eb9bbfcda15f98a713
Quellennotizuspto-grants-2014_10