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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 334348생성일: 2026년 10월 24일

Hydrogen Peroxide → (1RS,3RS,4RS)-3-(3,4-dimethoxyphenyl)-4-nitrocyclohexanol

https://huagongshe.com/ko/reaction/334348

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물PhosphateHCID 1061—
반응물Potassium;tri(butan-2-yl)boranuideHCID 4304157—
반응물(3RS,4SR)-3-(3,4-dimethoxyphenyl)-4-nitrocyclohexanoneHCID 67022408—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(1RS,3RS,4RS)-3-(3,4-dimethoxyphenyl)-4-nitrocyclohexanolHCID 17989075—

반응 조건

온도78 °C

반응 단계

Under nitrogen atmosphere 16.76 g of (3RS,4SR)-3-(3,4-dimethoxyphenyl)-4-nitrocyclohexanone (compound F2) are dissolved in 300 ml of tetrahydrofurane, the solution is cooled to 78° C., and 75 ml of 1 M solution of potassium tri-sec-butylborohydride in tetrahydrofurane is added dropwise. After stirring for further 1 h, a mixture consisting of 30% hydrogen peroxide solution and phosphate buffer solution is added. Stirring is continued for further 10 min, the reaction mixture is diluted with 400 ml of ethyl acetate and the aqueous layer is extracted with ethyl acetate, the combined organic phases are concentrated to give a foam, which is purified by chromatography on silica gel using a mixture of petroleum ether/ethyl acetate in the ratio 1/1 to furnish 10.18 g (60% of theory) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883818B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-c08233194c3142b88d6298b05a8b49fd
출처 메모uspto-grants-2014_11