HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 459076Erstellt: 24. Oktober 2026
Sodium Iodide → (2S)-2-Methoxy-3-{4-[3-(3-phenyl-benzofuran-6-yloxy)-prop-1-ynyl]-phenyl}-propionic acid
https://huagongshe.com/de/reaction/459076
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | 3-Phenyl-benzofuran-6-ol | HCID 12273525 | — |
| Edukt | (2S)-3-[4-(3-Chloro-prop-1-ynyl)-phenyl]-2-methoxy-propionic acid ethyl ester | HCID 58822943 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (2S)-2-Methoxy-3-{4-[3-(3-phenyl-benzofuran-6-yloxy)-prop-1-ynyl]-phenyl}-propionic acid | HCID 58822838 | — |
Reaktionsschritte
A solution of (2S)-3-[4-(3-Chloro-prop-1-ynyl)-phenyl]-2-methoxy-propionic acid ethyl ester from Step A (0.071 mmol, 1 eq) in 0.7 ml of DMF in a 16×100 mm tube treated with 3-phenyl-6-hydroxybenzofurane (0.078 mmol, 1.1 eq) Cesium Carbonate (0.213 mmol 3 eq) and NaI (0.071 mmol, 1 eq) and stirred at room temperature overnight. The reactants were filtered and washed with DMF several times. The solvent was evaporated under vacuo and the residue reconstituted in a mixture of Ethanol (2 ml) and NaOH (1M) (1 ml) and stirred at room temperature until reaction is completed by HPLC-MS. Then HCl (1M) was added (until pH=3) and the solvent were eliminated under vacuo. The residue was reconstituted in CH2Cl2/H2O and filtered through a hidrofobic syringer. The organic layer was separated, concentrated and purified by HPLC-MS to get the title compound. MS(ES) for C27H22O5 [M+H]+: 427.2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07192982B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-da13f274d6c3495a92c57a5ab0b9f326 |
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| Quellennotiz | uspto-grants-2007_03 |
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