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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247143생성일: 2026년 10월 25일

1,4-Naphthoquinone → 1,4,4a,9a-tetrahydro-1-[(2,3,6-trideoxy-4-O-p-nitrobenzoyl-3-trifluoroacetamido-alpha-L-lyxo-hexo-pyranosyl)methyl]-anthracene-9,10-dione

https://huagongshe.com/reaction/247143

반응식

참여 물질

역할이름HCID투입량
반응물1,4-NaphthoquinoneHCID 8530—
반응물(E)-1-(2,3,6-trideoxy-4-O-p-nitrobenzoyl-3-trifluoroacetamido-alpha-L-lyxo-hexopyranosyl)-2,4-pentadieneHCID 86741864—
용매TolueneHCID 1140—
생성물1,4,4a,9a-tetrahydro-1-[(2,3,6-trideoxy-4-O-p-nitrobenzoyl-3-trifluoroacetamido-alpha-L-lyxo-hexo-pyranosyl)methyl]-anthracene-9,10-dioneHCID 8674186365.4%

반응 조건

온도0 °C

반응 단계

Ninety mg (0.203 mmoles) of (E)-1-(2,3,6-trideoxy-4-O-p-nitrobenzoyl-3-trifluoroacetamido-α-L-lyxo-hexopyranosyl)-2,4-pentadiene and 22.0 mg (0.140 mmoles) of 1,4 naphthoquinone were mixed in 10 ml toluene and the mixture was heated under N2 at 80°-88° C. for 4 hr. The reaction was chilled to 0° C. and filtered to give 55 mg (65%) 1,4,4a,9a-tetrahydro-1-[(2,3,6-trideoxy-4-O-p-nitrobenzoyl-3-trifluoroacetamido-α-L-lyxo-hexo-pyranosyl)methyl]-anthracene-9,10-dione in impure form.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04705850
출처 데이터셋uspto-grants-1987_11
ORD IDord-98dcba6dc26745f0a09eb5fa0e55e70b
출처 메모uspto-grants-1987_11