HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14002Erstellt: 23. Oktober 2026
Potassium Carbonate → Methyl 3-((dipropylamino)carbonyl]-5-ethylbenzoate
https://huagongshe.com/de/reaction/14002
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Lithium Chloride | HCID 433294 | — |
| Edukt | Ethylboronic acid | HCID 521157 | — |
| Edukt | Methyl 3-bromo-5-(dipropylcarbamoyl)benzoate | HCID 21939662 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Methyl 3-((dipropylamino)carbonyl]-5-ethylbenzoate | HCID 22593628 | — |
Reaktionsschritte
Ethylboronic acid (0.800 g, 10.8 mmol), dichlorobis(triphenylphosphine)-palladium(II) (0.252 g, 0.360 mmol), potassium carbonate (2.50 g, 18.0 mmol) and lithium chloride (0.151 g, 3.60 mmol) are added to a mixture of methyl 3-bromo-5-[(dipropylamino)carbonyl]benzoate (1.23 g, 3.60 mmol) in dry DMF (20 mL). The mixture is heated at 100 degrees C. for 18 hours. The mixture is then partitioned between ethyl acetate and water. The phases are separated and the ethyl acetate phase is washed with saline, dried over sodium sulfate and concentrated. The concentrate is column chromatographed (silica gel; ethyl acetate/hexanes, 15/85) to give the title compound, MS (ESI+) for C17H25NO3 m/z (M+H)+=292.2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07727997B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-87b264a8e2c347b0ba0c3634ea5dddab |
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| Quellennotiz | uspto-grants-2010_06 |
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