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HRID 1591210作成日:2026年10月27日

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

https://huagongshe.com/reaction/1591210

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphoric AcidHCID 1004—
反応物Sodium CyanideHCID 8929—
反応物1(2H)-Naphthalenone, 2-bromo-3,4-dihydro-HCID 101120—
反応物6-Bromo-2-tetraloneHCID 2733553—
反応物1-Oxo-1,2,3,4-tetrahydro-naphthalene-2-carbonitrileHCID 12231027—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒AcetonitrileHCID 6342—
生成物6-Oxo-5,6,7,8-tetrahydronaphthalene-2-carbonitrileHCID 16244504—

反応条件

温度80 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05206240
出典データセットuspto-grants-1993_04
ORD IDord-62efd930a94c464ebc0d4e6077652372
出典メモuspto-grants-1993_04