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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175712Generated: November 2, 2026

Triethylamine → Ethyl 2-(2-iodo-4,5-dimethoxybenzamido)acetate

https://huagongshe.com/reaction/2175712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-Iodo-4,5-dimethoxybenzoic acidHCID 2758422—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-(2-iodo-4,5-dimethoxybenzamido)acetateHCID 6708780595%

Reaction Steps

To a stirred solution of 2-iodo-4,5-dimethoxybenzoic acid (24.6 g, 80 mmol), ethyl 2-aminoacetate hydrochloride (11 g, 88 mmol), EDCl (17 g, 88 mmol) and HOBt (14 g, 88 mmol) in dry DCM (500 mL) was added Et3N (55 mL, 400 mmol) dropwise at rt. The resulting mixture was stirred at room temperature overnight then the reaction was quenched with water, and thoroughly extracted with DCM. The combined organic phases were washed with brine and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by flash chromatography using petroleum ether/ethyl acetate 3:1 (v:v) as eluent to give ethyl 2-(2-iodo-4,5-dimethoxybenzamido)acetate (29 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062076B2
Source datasetuspto-grants-2015_06
ORD IDord-69c2e5e7112d483f807a47575309e914
Source noteuspto-grants-2015_06