Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926265Generated: October 25, 2026

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

https://huagongshe.com/reaction/926265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant3-Methoxy-2-methyl-3-oxopropanoic acidHCID 300693—
Reactant2-(2-Iodophenyl)ethanamineHCID 10514616—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-((2-iodophenethyl)amino)-2-methyl-3-oxopropanoateHCID 8671134378.5%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284331B2
Source datasetuspto-grants-2016_03
ORD IDord-f8688558e29c4735b0c40bd716b90d10
Source noteuspto-grants-2016_03