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HRID 334348作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物PhosphateHCID 1061—
反応物Potassium;tri(butan-2-yl)boranuideHCID 4304157—
反応物(3RS,4SR)-3-(3,4-dimethoxyphenyl)-4-nitrocyclohexanoneHCID 67022408—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物(1RS,3RS,4RS)-3-(3,4-dimethoxyphenyl)-4-nitrocyclohexanolHCID 17989075—

反応条件

温度78 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883818B2
出典データセットuspto-grants-2014_11
ORD IDord-c08233194c3142b88d6298b05a8b49fd
出典メモuspto-grants-2014_11