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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 359401Erstellt: 23. Oktober 2026

O-Xylene → 1-(4-Fluorophenyl)-4-oxocyclohexanecarbonitrile

https://huagongshe.com/de/reaction/359401

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktO-XyleneHCID 7237—
EduktMethyl AcrylateHCID 7294—
EduktBenzeneacetonitrile, 4-fluoro-HCID 68016—
EduktSodium MethoxideHCID 10942334—
Produkt1-(4-Fluorophenyl)-4-oxocyclohexanecarbonitrileHCID 91805—

Reaktionsschritte

A mixture of 221 parts of 4-fluorobenzeneacetonitrile, 700 parts of sodium methoxide solution 30% and 900 parts of dimethylbenzene was stirred for 5 minutes. Then there were added dropwise 309 parts of methyl 2-propenoate (exothermic reaction: temperature rose to 65° C.). Upon completion, stirring was continued overnight at reflux temperature. The methanol was distilled off till an internal temperature of 110° C. was reached. After cooling, 1000 parts of a hydrochloric acid solution 6N were added dropwise and the whole was stirred and refluxed for 5 minutes. Upon cooling, the layers were separated. The organic phase was dried, filtered and evaporated. The residue was stirred and refluxed for 4 hours together with 500 parts of acetic acid, 500 parts of water and 500 parts of a hydrochloric acid solution. After cooling, the product was extracted with trichloromethane. The extract was washed successively with water, with a diluted sodium hydroxide solution and again with water till neutralization, dried, filtered and evaporated. The residue was crystallized from 2-propanol, yielding 134.5 parts of 1-(4-fluorophenyl)-4-oxocyclohexanecarbonitrile; mp. 91.8° C. (intermediate 1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05001125
Quelldatensatzuspto-grants-1991_03
ORD IDord-f87bb568ddf449ee9d83b9b9813a5e7b
Quellennotizuspto-grants-1991_03