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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1105878생성일: 2026년 10월 26일

Triethylamine → 6-(5-Cholesten-3beta-yloxy)hexyl 2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranoside

https://huagongshe.com/reaction/1105878

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물6-(5-Cholesten-3beta-yloxy)hexyl iodideHCID 12805525—
반응물2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranoseHCID 23238908—
용매DichloromethaneHCID 6344—
생성물6-(5-Cholesten-3beta-yloxy)hexyl 2,3,4-tri-O-acetyl-1-thio-beta-L-fucopyranosideHCID 13171264361%

반응 단계

2,3,4-Tri-O-acetyl-1-thio-β-L-fucopyranose (10 mmol) is treated with 6-(5-cholesten-3β-yloxy)hexyl iodide (10 mmol) in dichloromethane (30 ml) containing triethylamine (10 mmol). The reaction takes place in 1 day at room temperature under nitrogen. The resulting solution is washed with distilled water (20 ml) and dried with anhydrous sodium sulfate. The filtered solution is concentrated to form a syrup which is put on a silica gel column and eluted with chloroform followed by 1.0% ethanol in chloroform. The fractions containing the title compound, as determined by thin layer chromatography, are pooled and evaporated to give the title compound in 61% yield [α]D -4° (c 1.5, chloroform).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04310505
출처 데이터셋uspto-grants-1982_01
ORD IDord-11d0510d869e4df58af621773eb555f4
출처 메모uspto-grants-1982_01