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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 466905생성일: 2026년 10월 25일

2,4,6-Trimethylpyridine → Methyl 6-O-(4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl)-2,3,4-tri-O-benzyl-alpha-D-glucopyranoside

https://huagongshe.com/reaction/466905

반응식

참여 물질

역할이름HCID투입량
반응물2,4,6-TrimethylpyridineHCID 7953—
반응물Methyl 2,3,4-tri-O-benzyl-alpha-D-glucopyranosideHCID 11190476—
반응물4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl chlorideHCID 54403365—
촉매Silver perchlorateHCID 24562—
용매Diethyl EtherHCID 3283—
생성물Methyl 6-O-(4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl)-2,3,4-tri-O-benzyl-alpha-D-glucopyranosideHCID 53849711—

반응 조건

온도-30 °C

반응 단계

Ethereal silver perchlorate (0.08 M, 76.9 mL, 6.15 mmol) is added with stirring at -30° C. to a solution of methyl 2,3,4-tri-O-benzyl-α-D-glucopyranoside (2.078 g, 4.48 mmol), 4-O-acetyl-2,3,6-tri-O-benzyl-α-D-galactopyranosyl chloride (2.859 g, 5.6 mmol) and 2,4,6-trimethylpyridine (0.81 mL, 6.15 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 6-O-(4-O-acetyl-2,3,6-tri-O-benzyl-α-D-galactopyranosyl)-2,3,4-tri-O-benzyl-α-D-glucopyranoside as a foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05157116
출처 데이터셋uspto-grants-1992_10
ORD IDord-ea2e577b99044a9fbcce7033137ab7e9
출처 메모uspto-grants-1992_10