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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643040Generated: October 25, 2026

2-Aminopropanol → N-(2-hydroxy-1-methyl-ethyl)-3-iodobenzamide

https://huagongshe.com/reaction/643040

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopropanolHCID 5126—
ReactantTriethylamineHCID 8471—
Reactant3-Iodobenzoic acidHCID 12060—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
SolventDichloromethaneHCID 6344—
ProductN-(2-hydroxy-1-methyl-ethyl)-3-iodobenzamideHCID 2373007634%

Reaction Steps

To a solution of 3-iodobenzoic acid (10.02 g, 40.30 mmol), in dry dichloromethane, at room temperature (180 mL) under a nitrogen atmosphere, EDCI (7.72 g, 40.30 mmol) was added followed by triethylamine (8.0 mL, 60.45 mmol) and the mixture was stirred at room temperature for further 5 minutes. DL Alaninol (3.02 g, 40.3 mmol) was then added and the mixture stirred at room temperature for 16 hrs. The reaction mixture was washed with a mixture of saturated brine and saturated sodium bicarbonate (1:1; 2×150 mL) followed by saturated brine solution (100 mL). The organics were separated and dried over magnesium sulfate and the solvent evaporated under vacuum. The residue was purified by flash column chromatography on silica gel (DCM:MeOH, 1% to 8% methanol gradient) to afford compound 1 (4.14 g, 13.6 mmol, 34% yield) as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696382B2
Source datasetuspto-grants-2010_04
ORD IDord-c4a65e7e43f94ca0b5a432db548271d9
Source noteuspto-grants-2010_04