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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 224735생성일: 2026년 10월 23일

Ammonium cerium-nitrate → (S)-(+)-5-(3,4-dihydroxy-3-methyl-1-butyl)-2,3,6-trimethyl-p-benzoquinone

https://huagongshe.com/ko/reaction/224735

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium cerium-nitrateHCID 57418452—
반응물(S)-4-(3,5-dimethoxy-3,4,6-trimethyl-phenylethyl)-2,2,4-trimethyl-1,3-dioxolanHCID 70593036—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물(S)-(+)-5-(3,4-dihydroxy-3-methyl-1-butyl)-2,3,6-trimethyl-p-benzoquinoneHCID 1310053641.4%

반응 단계

While stirring for 2 minutes at room temperature, 2.01 g of cerium ammonium nitrate in 7.5 ml of water were added dropwise to a solution of 550 mg of (S)-4-(3,5-dimethoxy-3,4,6-trimethyl-phenylethyl)-2,2,4-trimethyl-1,3-dioxolan in 7.5 ml of acetonitrile. After 2 minutes of additional stirring, the reaction mixture was extracted three times with 20 ml of chloroform each time. The combined organic extracts were dried over sodium sulfate, whereafter the solvent was removed. After chromatography of the obtained residue on silica gel with benzene/ethyl acetate (2:1 parts by volume) and ethyl acetate, there were obtained 266 mg of (S)-(+)-2,3,6-trimethyl-5-(2,2,4-trimethyl-1,3-dioxolan-4-ethyl)-p-benzoquinone and 177 mg of (S)-(+)-5-(3,4-dihydroxy-3-methyl-1-butyl)-2,3,6-trimethyl-p-benzoquinone in the form of yellow needles with a melting point of 111°-112°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04234490
출처 데이터셋uspto-grants-1980_11
ORD IDord-12f2e00f35a244c6bc18dd4018a4c9b1
출처 메모uspto-grants-1980_11