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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| 반응물 | Methyl 2,3,4-tri-O-benzyl-alpha-D-glucopyranoside | HCID 11190476 | — |
| 반응물 | 4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl chloride | HCID 54403365 | — |
| 촉매 | Silver perchlorate | HCID 24562 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | Methyl 6-O-(4-O-acetyl-2,3,6-tri-O-benzyl-alpha-D-galactopyranosyl)-2,3,4-tri-O-benzyl-alpha-D-glucopyranoside | HCID 53849711 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05157116 |
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| 출처 데이터셋 | uspto-grants-1992_10 |
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| ORD ID | ord-ea2e577b99044a9fbcce7033137ab7e9 |
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| 출처 메모 | uspto-grants-1992_10 |
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