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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Aminopropanol | HCID 5126 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Iodobenzoic acid | HCID 12060 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-hydroxy-1-methyl-ethyl)-3-iodobenzamide | HCID 23730076 | 34% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696382B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-c4a65e7e43f94ca0b5a432db548271d9 |
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| Source note | uspto-grants-2010_04 |
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