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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2911생성일: 2026년 10월 23일

4-Benzyloxy-6-[2-(3,4-dibenzyloxyphenyl)-2-hydroxyethyl]-2H-pyran-2-one → 4-Hydroxy-6-[2-(3,4-dihydroxyphenyl)-2-hydroxyethyl]-2H-pyran-2-one

https://huagongshe.com/ko/reaction/2911

반응식

참여 물질

역할이름HCID투입량
반응물4-Benzyloxy-6-[2-(3,4-dibenzyloxyphenyl)-2-hydroxyethyl]-2H-pyran-2-oneHCID 19688074—
반응물HCID 178418361HCID 178418361—
촉매NickelHCID 935—
용매EthanolHCID 702—
생성물4-Hydroxy-6-[2-(3,4-dihydroxyphenyl)-2-hydroxyethyl]-2H-pyran-2-oneHCID 8675232070%

반응 단계

35.6 g (66.6 mmol) 4-benzyloxy-6-[2-[3,4-dibenzyloxyphenyl)-2-hydroxy-ethyl)]-2H-pyran-2-one (VI) was hydrogenated for 6 hours at room temperature under a hydrogen pressure of 44 mbar in 1200 ml ethanol using 10 g W2 Raney nickel. After taking up 4.4 l hydrogen the catalyst was removed by suction filtration and it was rewashed several times with tetrahydrofuran. The evaporated filtrates yielded 12.2 g (70%) VII after triturating with ether, melting point 153° C. (decomp.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731344
출처 데이터셋uspto-grants-1998_03
ORD IDord-65ca9c80774841d78cc6437f7406abeb
출처 메모uspto-grants-1998_03