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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1720183생성일: 2026년 10월 24일

Diethyl Ether → Methyl 4-O-(2,3,6-tri-O-benzyl-4-deoxy-4-acetyloxymethy-alpha-D-glucopyranosyl)-2,3,6-tri-O-benzyl-alpha-D-glucopyranoside

https://huagongshe.com/ko/reaction/1720183

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물(2R,3R,4S,5R,6S)-6-methoxy-4,5-bis(phenylmethoxy)-2-(phenylmethoxymethyl)oxan-3-olHCID 10983459—
촉매Silver perchlorateHCID 24562—
생성물Methyl 4-O-(2,3,6-tri-O-benzyl-4-deoxy-4-acetyloxymethy-alpha-D-glucopyranosyl)-2,3,6-tri-O-benzyl-alpha-D-glucopyranosideHCID 54010971—

반응 조건

온도-30 °C

반응 단계

Ethereal silver perchlorate (0.08 M, 9.58 ml, 7.67 mmol) is added with stirring at -30° C. to a solution of methyl 2,3,6-tri-O-benzyl-α-D-glucopyranoside (2.592 g, 5.59 mmol), 2,3,6-tri-O-benzyl-1,4-dideoxy-4-acetyloxymethyl-D-gluco-pyranosyl chloride (3.661 g, 6.98 mmol) in ether (20 ml). The mixture is stirred 15 min at -30° C. and silver chloride precipitated. The mixture is filtered through a celite pad, the solids are washed with ether, the filtrate is concentrated under reduced pressure. The residue is dissolved in methylene chloride and the organic layer is washed successively with aqueous sodium thiosulfate and water. The organic layer is dried over sodium sulfate, filtered and concentrated under reduced pressure so as to afford a foam. Flash chromatography on silica gel and elution with a graded mixture of hexane and ethyl acetate will afford methyl 4-O-(2,3,6-tri-O-benzyl-4-deoxy-4-acetyloxymethyl-α-D-glucopyranosyl)-2,3,6-tri-O-benzyl-α-D-glucopyranoside as a foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05504078
출처 데이터셋uspto-grants-1996_04
ORD IDord-46742bde2673474babe503b8a971d1dd
출처 메모uspto-grants-1996_04