Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1684332Erstellt: 26. Oktober 2026

Dichloromethane → 4-Cyano-6,7-dimethyl-1-indanone

https://huagongshe.com/reaction/1684332

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt4-Bromo-6,7-dimethyl-2,3-dihydro-1H-inden-1-oneHCID 13809869—
EduktHCID 178418546HCID 178418546—
KatalysatorTrichloroiron;hexahydrateHCID 16211236—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-Cyano-6,7-dimethyl-1-indanoneHCID 19042293—

Reaktionsschritte

A mixture of 17.8 g (74.5 mmol) of 4-bromo-6,7-dimethyl-1-indanone [J. Het. Chem. 24, 677 (1987)] and 7.3 g (82 mmol) of copper(I) cyanide in 18 ml of DMF is stirred for 6 hours at 170°. The reaction mixture is then cooled to 100° and 200 ml of toluene and a solution of 31.2 g of iron(III) chloride hexahydrate in 47 ml of water and 8.2 ml of concentrated hydrochloric acid are added in succession thereto. The reaction mixture is stirred for 20 minutes at 70°, cooled and diluted with toluene and water. The organic phase is separated off, washed with water, a semi-saturated sodium hydrogen carbonate solution and again with water, dried and concentrated by evaporation. The residue is crystallised from ethyl acetate and ether and corresponds to starting compound (a). Beige crystals having a melting point of 160°-163° are obtained; IR (CH2Cl2): 2220, 1710 cm-1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05639911
Quelldatensatzuspto-grants-1997_06
ORD IDord-44d76b1b0c854e49ad1f62898b5acea8
Quellennotizuspto-grants-1997_06