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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395585Erstellt: 24. Oktober 2026

Fluorobenzene → Methyl 6-(4-fluorophenyl)-6-oxohexanoate

https://huagongshe.com/de/reaction/395585

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFluorobenzeneHCID 10008—
EduktMethyl 6-chloro-6-oxohexanoateHCID 520737—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 6-(4-fluorophenyl)-6-oxohexanoateHCID 69905189—

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

A suspension of 2.59 g (19.4.10−3 mol) of aluminum chloride in 4 ml of dichloromethane is prepared. It is cooled to −5° C. and a mixture of 0.97 ml (10.3.10−3 mol) of fluorobenzene and 1.31 ml (8.4.10−3 mol) of methyl 6-chloro-6-oxohexanoate in 3 ml of dichloromethane is added gradually, the temperature being maintained between −4 and −7° C. The temperature is then allowed to rise to 20° C. and, after 15 hours, the mixture is hydrolyzed in acidified iced water. It is extracted with dichloromethane and the organic phase obtained is washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The 2 g of crude product recovered in this way are purified by chromatography on silica gel using a petroleum ether/ethyl acetate mixture (96/4) as the eluent to give 1.26 g of the expected product in the form of a white powder (yield=63%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605633B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-4a0976bcd5cf4adeb77cbdd025bb3b9f
Quellennotizuspto-grants-2003_08