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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1781411생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1781411

반응식

참여 물질

역할이름HCID투입량
반응물Phosphoric AcidHCID 1004—
반응물Sodium CyanideHCID 8929—
반응물1(2H)-Naphthalenone, 2-bromo-3,4-dihydro-HCID 101120—
반응물6-Bromo-2-tetraloneHCID 2733553—
반응물1-Oxo-1,2,3,4-tetrahydro-naphthalene-2-carbonitrileHCID 12231027—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매AcetonitrileHCID 6342—
생성물6-Oxo-5,6,7,8-tetrahydronaphthalene-2-carbonitrileHCID 16244504—

반응 조건

온도80 °C

반응 단계

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 silfca 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05633247
출처 데이터셋uspto-grants-1997_05
ORD IDord-71eeed9b844b4aeeb9efd514647a519b
출처 메모uspto-grants-1997_05