HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249919Erstellt: 25. Oktober 2026
Tetrahydrofuran → Methyl 2-amino-5-methoxy-3-methylbenzoate
https://huagongshe.com/reaction/249919
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Methylboronic Acid | HCID 139377 | — |
| Edukt | Potassium Fluoride | HCID 522689 | — |
| Edukt | Tri-t-butylphosphonium | HCID 4060964 | — |
| Edukt | Methyl 2-amino-5-bromo-3-methoxybenzoate | HCID 13894022 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Produkt | Methyl 2-amino-5-methoxy-3-methylbenzoate | HCID 20281873 | 73% |
Reaktionsschritte
A mixture of methyl 2-amino-5-bromo-3-methoxybenzoate (6.50 g, 25 mmol), methylboronic acid (3.0 g, 50 mmol), potassium fluoride (5.8 g, 100 mmol) and tri-t-butylphosphonium tetrafluoroborte (0.87 g, 3.0 mmol) in THF (200 mL) was deoxygenated and then backfilled with argon. Tris(dibenzylideneacetone)dipalladium(0) (1.43 g, 1.5 mmol), was added and the mixture was heated at 70° C. for 17 h under an argon atmosphere. The reaction mixture was concentrated and the residue purified by column chromatography (silica gel, 0% to 5% EtOAc in hexanes) to afford methyl 2-amino-5-methoxy-3-methylbenzoate (3.55 g, 73%) 1H NMR consistent.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07863271B2 |
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| Quelldatensatz | uspto-grants-2011_01 |
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| ORD ID | ord-35df134f9a174ac298eb7dd43559fd3c |
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| Quellennotiz | uspto-grants-2011_01 |
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