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Potassium Cyanide → 6-Cyano-4-chromanone

HRID 1269440
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1269440
FC(F)(F)S(O[C:7]1[CH:16]=[C:15]2[C:10]([C:11](=[O:17])[CH2:12][CH2:13][O:14]2)=[CH:9][CH:8]=1)(=O)=O.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[C-:39]#[N:40].[K+]>CC#N.Cl.O.CC(C)=O.CCOCC.[Zn]>[C:39]([C:7]1[CH:16]=[C:15]2[C:10]([C:11](=[O:17])[CH2:12][CH2:13][O:14]2)=[CH:9][CH:8]=1)#[N:40]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

10

Edukt 3

HCID 9032Potassium CyanideHCID 11776TriphenylphosphineHCID 103571863,4-Dihydro-4-oxo-2H-1-benzopyran-7-yl 1,1,1-trifluoromethanesulfonate

Produkt 1

HCID 223499736-Cyano-4-chromanone

Reagenzien, Katalysatoren, Lösungsmittel 6

HCID 23994ZincKatalysator
HCID 180
Acetone
Lösungsmittel
HCID 313Hydrochloric AcidLösungsmittel
HCID 962WaterLösungsmittel
HCID 3283Diethyl EtherLösungsmittel
HCID 6342AcetonitrileLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

7-[[(Trifluoromethyl)sulfonyl]oxy]-4-chromanone (27.8 g, 94 mmol) and PPh3 (2.5g, 9.6 mmol) were dissolved in degassed CH3CN (350 mL). KCN (6.8 g, 105 mmol), (PPh3)2NiBr2 (3.5 g, 4.7 mmol) and acid washed (stirred in 0.5 N HCl 1 min, washed successively with H2O, acetone, and Et2O) zinc dust (2.0 g, 31 mmol) were added and the reaction was purged with N2. The reaction was heated in a 60° C. bath for 6 h. The reaction was cooled, poured into H2O (400 mL) and extracted with EtOAc (3×300 mL). The organic layers were combined and washed with H2O (200 mL) and brine (150 mL). The solution was dried over MgSO4, filtered and concentrated in vacuo to provide a residue which was purified on a plug of silica (CH2Cl2 eluant) to provide the title compound.

Aufarbeitung

  1. additionwere added
  2. customthe reaction was purged with N2
  3. temperatureThe reaction was cooled
  4. additionpoured into H2O (400 mL)
  5. extractionextracted with EtOAc (3×300 mL)
  6. washwashed with H2O (200 mL) and brine (150 mL)
  7. dry with materialThe solution was dried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customto provide a residue which
  11. customwas purified on a plug of silica (CH2Cl2 eluant)

Quellen und Nachweise

ORD-Eintrag
ord-3ba5a1d4ff704422bee76f7741b124c8
Quelldatensatz
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07199244B2

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