HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 535675Erstellt: 24. Oktober 2026
Methyl chloroacetate → 7-Bromo-5-fluorobenzofuran-2-carboxylic acid
https://huagongshe.com/de/reaction/535675
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl chloroacetate | HCID 7295 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 3-Bromo-5-fluoro-2-hydroxybenzaldehyde | HCID 23148955 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 7-Bromo-5-fluorobenzofuran-2-carboxylic acid | HCID 17982701 | 63% |
Reaktionsschritte
Methyl chloroacetate (7.6 mL, 86.8 mmol) was added to a mixture of 3-bromo-5-fluoro-2-hydroxy-benzaldehyde (9.5 g, 43.4 mmol), tetra-N-butyl-ammonium iodide (1.6 g, 4.34 mmol) and anhydrous potassium carbonate (24 g, 174 mmol). The reaction mixture was heated at 130° C. for 4 h, cooled to 0° C., diluted with tetrahydrofuran (100 mL) and then potassium hydroxide (17 g, 303 mmol) in water (100 mL). The mixture was stirred at rt for 18 h and then, concentrated under reduced pressure. The residue was acidified with HCl and extracted with ethyl acetate. The combined organic extracts were dried (Na2SO4), filtered and concentrated under reduced pressure. The crude compound was purified by flash chromatography (SiO2; toluene/EtOAc, 40/1) to give 7.0 g (63%) of the product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08859534B2 |
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| Quelldatensatz | uspto-grants-2014_10 |
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| ORD ID | ord-5e519e47b4254bf38cafbd0db2f6a7ce |
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| Quellennotiz | uspto-grants-2014_10 |
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