HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20453Erstellt: 26. Oktober 2026
Dimethylformamide → 3-Bromo-5-fluorobenzaldehyde
https://huagongshe.com/reaction/20453
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 1,3-Dibromo-5-fluorobenzene | HCID 137003 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-Bromo-5-fluorobenzaldehyde | HCID 21986246 | 55,3% |
Reaktionsschritte
Add dropwise a solution of 1,3-dibromo-5-fluorobenzene (12.39 mL, 98.5 mmol) in tetrahydrofuran (20 mL) to a solution of n-butyllithium (64.61 mL, 103.4 mmol, 1.6 M in hexanes) in tetrahydrofuran (55 mL) at −78° C. Stir at −78° C. for 45 minutes, add dimethylformamide (7.62 mL, 98.5 mmol), stir at −78° C. for 1.5 hours, remove cooling bath and stir 10 minutes. Add saturated aqueous ammonium chloride (150 mL) and extract with diethyl ether (2×700 mL). Wash combined organic layers sequentially with water (1×300 mL) and saturated aqueous sodium chloride (1×300 mL). Dry over magnesium sulfate and concentrate under reduced pressure. Subject residue to silica gel chromatography, eluting with 0-10% ethyl acetate in hexanes to provide the desired compound (11.05 g, 55.3%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745438B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-b4e139e6572d4378a1be70b4ffd45f05 |
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| Quellennotiz | uspto-grants-2010_06 |
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