Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Fluoro-3-nitrobenzene | HCID 9823 | — |
| Edukt | Chlorosuccinimide | HCID 31398 | — |
| Edukt | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-Chloro-1-fluoro-3-nitrobenzene | HCID 88883 | 9,3% |
Reaktionsschritte
To a −78° C. solution of 3-fluoronitrobenzene (2 g, 14.2 mmol) in THF (30 mL) was added N-chlorosuccinimide (5.69 g, 42.6 mmol) in THF (20 mL), NaHMDS (1 M in THF, 28.4 mL, 28.4 mmol) was then added dropwise to maintain an internal temperature below −75° C. The resulting mixture was stirred for 30 min at −78° C. Then it was partitioned between 5% of HCl and ethyl acetate. The combined organic layer is dried over MgSO4 and filtered. The solvent was evaporated and chromatography of the resulting solid on silica gel (20% Ethyl acetate Hexane) gave the desired product(231 mg, 9.2%). EI-MS m/z 176.5 (M+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06500863B1 |
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| Quelldatensatz | uspto-grants-2002_12 |
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| ORD ID | ord-024e256dfd614b48956879219a3257c2 |
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| Quellennotiz | uspto-grants-2002_12 |
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