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

HRID 1608581
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1608581
Br[C:2]1[CH:10]=[C:9]([CH3:11])[C:8]([CH3:12])=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2=[O:13].[Cu][C:15]#[N:16].C(Cl)Cl>CN(C=O)C.O.Cl.C1(C)C=CC=CC=1.O.O.O.O.O.O.[Fe](Cl)(Cl)Cl>[C:15]([C:2]1[CH:10]=[C:9]([CH3:11])[C:8]([CH3:12])=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2=[O:13])#[N:16]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 3

HCID 6344DichloromethaneHCID 138098694-Bromo-6,7-dimethyl-2,3-dihydro-1H-inden-1-oneHCID 178418546HCID 178418546, Verbindung

Produkt 1

HCID 190422934-Cyano-6,7-dimethyl-1-indanone

Reagenzien, Katalysatoren, Lösungsmittel 5

HCID 16211236Trichloroiron;hexahydrateKatalysator
HCID 313
Hydrochloric Acid
Lösungsmittel
HCID 962WaterLösungsmittel2×
HCID 1140TolueneLösungsmittel2×
HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  1. temperatureThe reaction mixture is then cooled to 100°
  2. stirringThe reaction mixture is stirred for 20 minutes at 70°
  3. temperaturecooled
  4. customThe organic phase is separated off
  5. washwashed with water
  6. dry with materiala semi-saturated sodium hydrogen carbonate solution and again with water, dried
  7. concentrationconcentrated by evaporation
  8. customThe residue is crystallised from ethyl acetate and ether and corresponds
  9. customare obtained

Quellen und Nachweise

ORD-Eintrag
ord-055e89f5667443358541f709247e6755
Quelldatensatz
uspto-grants-1995_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05395855

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