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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9262Erstellt: 24. Oktober 2026

Boron trifluoride etherate → 8-Fluoro-1-tetralone

https://huagongshe.com/de/reaction/9262

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron trifluoride etherateHCID 8000—
EduktTert-Butyl nitriteHCID 10906—
Edukt8-Amino-1-tetraloneHCID 11400942—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelPentaneHCID 8003—
Produkt8-Fluoro-1-tetraloneHCID 11252188—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

The amine (Intermediate J3, 1.83 g, 11.3 mmol) in CH2Cl2 (17 mL) was added to BF3.OEt2 (2.80 mL, 22.1 mmol) at −15° C. More CH2Cl2 (20 mL) was added to the precipitate. Next, t-butyl nitrite (1.8 mL, 12.9 mmol) in CH2Cl2 (20 mL) was added at −15° C. and stirred for 10 min. and at 0° C. for 20 m. The mixture was diluted with pentane (40 mL), filtered and the solids were collected, washed with ether, and dried under vacuum. The solids were placed in a flask and heated to 115° C. for 10–15 min. followed by addition of 2N NaOH and CHCl3. The suspension was filtered and the aqueous phase was extracted with CHCl3. The organic layers were combined, dried over MgSO4, filtered and purified by chromatography on SiO2 with 15% EtOAc:Hx. The product, 8-fluoro-3,4-dihydro-2H-naphthalen-1-one (Intermediate J4) was isolated; 750 mg (40%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091232B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-a8ca59da901b4226a81b5c7540f40e6a
Quellennotizuspto-grants-2006_08