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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1591210Erstellt: 26. Oktober 2026

Phosphoric Acid → 6-Oxo-5,6,7,8-tetrahydronaphthalene-2-carbonitrile

https://huagongshe.com/reaction/1591210

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphoric AcidHCID 1004—
EduktSodium CyanideHCID 8929—
Edukt1(2H)-Naphthalenone, 2-bromo-3,4-dihydro-HCID 101120—
Edukt6-Bromo-2-tetraloneHCID 2733553—
Edukt1-Oxo-1,2,3,4-tetrahydro-naphthalene-2-carbonitrileHCID 12231027—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelAcetonitrileHCID 6342—
Produkt6-Oxo-5,6,7,8-tetrahydronaphthalene-2-carbonitrileHCID 16244504—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A flame dried 1 liter round bottom flask with argon inlet, digital thermometer, and magnetic stir bar, was charged with a 68% NaCN/alumina mixture (21.22 g, 433 mmol)(NaCN and alumina were ground together in a morter and pestle according to the procedure of Dalton et al. J. Org. Chem., 44, (24) 4443(1979)), and tetrakis (triphenylphospine) palladium(0) (10.0 g, 8.65 mmol). The flask was purged three times via vacuum with argon and a solution of 6-bromo-2-tetralone (19.46 g, 86.5 mmol) in degassed toluene (400 mL) was added. The mixture was heated to 80° C. and stirred for 64 hrs at that temperature. Analysis by HPLC indicated 89% conversion (HPLC conditions, column: Waters C18 Bondapak, eluent: 80:20 (0.1% H3PO4 in H2O: CH3CN), flow: 2 mL/min, wavelength: 220 nm, Rt: bromotetralone =9.65 min, cyanotetralone=3.46 min). The reaction was cooled and the mixture filtered through silica gel (elution with 60% ethyl acetate in hexane.) Concentration of the appropriate fractions gave 9.4 g (68%) of 6-cyano-2-tetralone (98.7% by HPLC).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05206240
Quelldatensatzuspto-grants-1993_04
ORD IDord-62efd930a94c464ebc0d4e6077652372
Quellennotizuspto-grants-1993_04