HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 330760Erstellt: 24. Oktober 2026
Ethyl 3,4-Diaminobenzoate → 4-Methoxycarbonylphenylboronic acid
https://huagongshe.com/de/reaction/330760
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl 3,4-Diaminobenzoate | HCID 458855 | — |
| Edukt | Potassium Acetate | HCID 517044 | — |
| Edukt | Bis(pinacolato)diborane | HCID 2733548 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 4-Methoxycarbonylphenylboronic acid | HCID 2734369 | 228,9% |
Reaktionsschritte
Referring to Scheme 11-1, to a solution of the bromide 1 (2.0 g, 4.2 mmol, prepared according to published conditions) in dioxane (60 mL) was added bis(pinacolato)diboron (4.32 g, 17 mmol), Pd(PPh3)4 (0.49 g, 0.42 mmol) and potassium acetate (2.06 g, 21 mmol) under nitrogen atmosphere. The reaction mixture was stirred at 80° C. for 5 h, and then diluted with ethyl acetate (150 mL). The organic phase was washed with H2O (20 mL), dried over sodium sulfate and concentrated in vacuo. The residue was further purified by silica gel column chromatography (haxanes/ethyl acetate=1/4 to 0/1 (v/v)) to give 2 (1.73 g, 79% yield). LC-MS (ESI): m/z 523.3 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08877707B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-a76ba1f3b0ac456bb8cdf65b35c10a73 |
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| Quellennotiz | uspto-grants-2014_11 |
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