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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37116생성일: 2026년 10월 23일

p-Toluenesulfonic acid → 6-cyano-3,4-dihydro-2,2-dimethyl-4-(6-oxo-1-cyclohexen-1-yl)-2H-1,4-benzoxazine

https://huagongshe.com/ko/reaction/37116

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물1,2-CyclohexanedioneHCID 13006—
반응물6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazineHCID 10535622—
용매TolueneHCID 1140—
생성물6-cyano-3,4-dihydro-2,2-dimethyl-4-(6-oxo-1-cyclohexen-1-yl)-2H-1,4-benzoxazineHCID 1049316566.7%

반응 단계

In 15 ml of toluene were dissolved 0.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazine, 0.33 g of cyclohexane-1,2-dione and a catalytic amount of p-toluenesulfonic acid and using a Dean-Stark trap, the solution was refluxed under heating for 4 hours. After cooling, the reaction mixture was washed with saturated aqueous sodium hydrogen carbonate solution and aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography and the resulting crude crystals were washed with ethanol to give 0.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-4-(6-oxo-1-cyclohexen-1-yl)-2H-1,4-benzoxazine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420126
출처 데이터셋uspto-grants-1995_05
ORD IDord-543880f311e840e5a659f21d25f74264
출처 메모uspto-grants-1995_05