HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 660571Erstellt: 25. Oktober 2026
2-Iodobenzoic acid → (2-Iodobenzoylamino)-(2-iodophenyl)-acetic Acid Methyl Ester
https://huagongshe.com/reaction/660571
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Iodobenzoic acid | HCID 6941 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Edukt | Methyl 2-amino-2-(2-iodophenyl)acetate | HCID 68840368 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (2-Iodobenzoylamino)-(2-iodophenyl)-acetic Acid Methyl Ester | HCID 68839341 | — |
Reaktionsschritte
To a solution of 2-iodobenzoic acid (6.4 g, 25.8 mmol) in THF (90 mL) is added HOBt (3.5 g, 25.8 mmol). After the mixture is stirred at RT for 10 min, EDCl (4.93 g, 25.8 mmol) is added followed by triethylamine (4.9 mL, 34.4 mmol). The mixture is stirred at RT for 40 min then amino-(2-iodophenyl)-acetic acid methyl ester (5.0 g, 17.2 mmol) is added and stirring is continued for 18 h. The solvent is removed under reduced pressure and water is added to the residue. The mixture is extracted with EtOAc and the organic phase is washed with brine and dried over magnesium sulfate. The solvent is removed under reduced pressure and the residue purified by flash chromatography using a gradient of 0-60% EtOAc/hexane as eluent to give the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08084448B2 |
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| Quelldatensatz | uspto-grants-2011_12 |
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| ORD ID | ord-45843441750b4de891869517c6bbf880 |
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| Quellennotiz | uspto-grants-2011_12 |
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