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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19792Erstellt: 26. Oktober 2026

Iodine → 2-Cyclopropyl-1-fluoro-4-iodobenzene

https://huagongshe.com/reaction/19792

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktIsoamyl NitriteHCID 8053—
EduktCesium iodideHCID 24601—
Edukt3-Cyclopropyl-4-fluoroanilineHCID 57416303—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt2-Cyclopropyl-1-fluoro-4-iodobenzeneHCID 6856411072%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of 3-cyclopropyl-4-fluorophenylamine (210 mg, 1.39 mmol) in DME (1.5 ml) was added caesium iodide (360 mg, 1.39 mmol), cuprous iodide (82 mg, 0.43 mmol), iodine (176 mg, 0.70 mmol) and isoamyl nitrite (1.11 ml, 8.34 mmol). The reaction mixture was heated to 60° C. for 2 h. The reaction mixture was cooled to RT and partitioned between pentane and sat. NH4Cl solution. The organic layer was separated, washed with 5% sodium thiosulfite and brine, dried (MgSO4), filtered and concentrated in vacuo to give a residue which was purified by flash column chromatography (100% pentane) to yield the desired 2-cyclopropyl-1-fluoro-4-iodobenzene (262 mg, 72%) as a colorless oil. 1H NMR (CDCl3, 300 MHz): 7.40 (m, 1H), 7.17 (m, 1H), 6.76 (m, 1H), 2.02 (m, 1H), 1.03-0.96 (m, 2H), 0.74-0.68 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745477B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-27835b63b9e04a92b1eee076253f85c2
Quellennotizuspto-grants-2010_06