HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49431Erstellt: 25. Oktober 2026
Methyl iodide → 3-Benzyloxy-6-methoxypicolinic acid
https://huagongshe.com/reaction/49431
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Edukt | Acetone hexane | HCID 21880519 | — |
| Edukt | Methyl 3-benzyloxy-6-methoxypicolinate | HCID 22175139 | — |
| Katalysator | HCID 178418647 | HCID 178418647 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 3-Benzyloxy-6-methoxypicolinic acid | HCID 17817634 | — |
Reaktionsschritte
To a stirred solution of this compound (10.25 g) in toluene (125 mL), warmed in an oil bath at 60° C., was added silver carbonate (16.6 g), then methyl iodide (8.52 g). The resulting mixture was stirred and heated for 3 hours at 60° C. After cooling, the mixture was filtered through Celite® and the solvent evaporated to give a yellow oil. Silica gel chromatography (4:1 hexane/acetone) gave a nearly colorless oil, whose 1H-NMR and MS data were consistent with methyl 3-benzyloxy-6-methoxypicolinate. Hydrolysis of this ester to the title acid 18 was accomplished with LiOH.H2O as described above for related esters.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06706740B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-f82f0be578eb468b9834a285f41dd5f3 |
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| Quellennotiz | uspto-grants-2004_03 |
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