HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1405404Erstellt: 24. Oktober 2026
Isobutyraldehyde trimethylsilyl enol ether → Benzyl 3-methoxy-4-(2-methyl-1-oxopropan-2-yl)benzoate
https://huagongshe.com/de/reaction/1405404
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isobutyraldehyde trimethylsilyl enol ether | HCID 99685 | — |
| Edukt | Benzyl 4-bromo-3-methoxybenzoate | HCID 58551480 | — |
| Katalysator | Zinc(II) fluoride | HCID 10129912 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Benzyl 3-methoxy-4-(2-methyl-1-oxopropan-2-yl)benzoate | HCID 86668528 | — |
Reaktionsschritte
To a flask purged with nitrogen was added Pd(tBu3P)2 (26 mg, 0.050 mmol), ZnF2 (52 mg, 0.50 mmol) and DMF (4 mL). The reaction mixture was allowed to stir for 10 minutes before benzyl 4-bromo-3-methoxy-benzoate (323 mg, 1.01 mmol) was added followed by trimethyl(2-methylprop-1-enoxy)silane (277 μL, 1.51 mmol). The reaction was heated at 80° C. overnight. The crude mixture was quenched with brine and extracted with EtOAc 3 times. The organic layer was dried over sodium sulfate and the solvent was evaporated to give benzyl 3-methoxy-4-(2-methyl-1-oxopropan-2-yl)benzoate. ESI-MS m/z calc. 312.4, found 313.4 (M+1)+; Retention time: 3.27 minutes (4 min run).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08916565B2 |
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| Quelldatensatz | uspto-grants-2014_12 |
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| ORD ID | ord-a69e54d1aad34fee997f6f535585fb9b |
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| Quellennotiz | uspto-grants-2014_12 |
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