HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 643040Erstellt: 24. Oktober 2026
2-Aminopropanol → N-(2-hydroxy-1-methyl-ethyl)-3-iodobenzamide
https://huagongshe.com/de/reaction/643040
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Aminopropanol | HCID 5126 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 3-Iodobenzoic acid | HCID 12060 | — |
| Edukt | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-(2-hydroxy-1-methyl-ethyl)-3-iodobenzamide | HCID 23730076 | 34% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07696382B2 |
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| Quelldatensatz | uspto-grants-2010_04 |
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| ORD ID | ord-c4a65e7e43f94ca0b5a432db548271d9 |
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| Quellennotiz | uspto-grants-2010_04 |
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