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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1629630생성일: 2026년 10월 25일

beta-D-Galactose pentaacetate → 2,3,4,6-tetra-O-acetyl-D-galactopyranose

https://huagongshe.com/reaction/1629630

반응식

참여 물질

역할이름HCID투입량
반응물beta-D-Galactose pentaacetateHCID 94752—
반응물Hydrazine, acetate (1:1)HCID 165591—
용매TetrahydrofuranHCID 8028—
생성물2,3,4,6-tetra-O-acetyl-D-galactopyranoseHCID 1105716298%

반응 단계

Under nitrogen atmosphere, hydrazine acetate (197 mg, 2.19 mmol, 1.4 equiv) was added to a solution of β-D-galactopyranose pentaacetate (605 mg, 1.55 mmol) in anhydrous THF (10 mL) in presence of 4 Å molecular sieve. The reaction mixture was stirred at room temperature for 4 h 30, filtered, concentrated to dryness under reduced pressure and purified by chromatography on silica gel (25:1, dichloromethane/methanol) to afford 2,3,4,6-tetra-O-acetyl-D-galactopyranose (528 mg, 98%) as a yellow oil which was directly used in the next step. Under nitrogen atmosphere, trichloroacetonitrile (1.34 mL, 13.4 mmol, 8.8 equiv) and potassium carbonate (1.42 g, 10.3 mmol, 6.7 equiv) were added to a solution of 2,3,4,6-tetra-O-acetyl-D-galactopyranose (528 mg, 1.52 mmol) in anhydrous dichloromethane (20 mL) in presence of 4 Å molecular sieve. The reaction mixture was vigourously stirred at room temperature for 12 h, filtered and concentrated to dryness under reduced pressure to afford 2,3,4,6-tetra-O-acetyl-α-D-galactopyranosyl trichloroacetamidate (707 mg, 95%) which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08790664B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-91817b81309741fb8d87bda8a8e4f9d8
출처 메모uspto-grants-2014_07