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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2301653Erstellt: 24. Oktober 2026

1-Fluoro-3-nitrobenzene → 2-Chloro-1-fluoro-3-nitrobenzene

https://huagongshe.com/de/reaction/2301653

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Fluoro-3-nitrobenzeneHCID 9823—
EduktChlorosuccinimideHCID 31398—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Chloro-1-fluoro-3-nitrobenzeneHCID 888839,3%

Reaktionsbedingungen

Temperatur-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06500863B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-024e256dfd614b48956879219a3257c2
Quellennotizuspto-grants-2002_12