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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6027생성일: 2026년 10월 24일

Ethanol → 4-cyanophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranoside

https://huagongshe.com/ko/reaction/6027

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물4-CyanophenolHCID 13019—
반응물2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
촉매ZincchlorideHCID 3007855—
촉매Silver imidazolateHCID 10931941—
용매DichloromethaneHCID 6344—
생성물4-cyanophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranosideHCID 15067846112.5%

반응 조건

온도40 °C

반응 단계

A suspension of 6.5 g (12.3.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide, 6 g (50.4.10-3 mol) of 4-hydroxybenzonitrile, 6.9 g (50.5.10-3 mol) of zinc chloride and 4.4 g (25.1.10-3 mol) of silver imidazolate in 200 ml of anhydrous methylene chloride is stirred at 40° C., under an inert atmosphere, in the absence of light and in the presence of a molecular sieve (400 pm). After 7 h at this temperature, 6.9 g (50.5.10-3 mol) of zinc chloride, 4.4 g (25.1.10-3 mol) of silver imidazolate and 6.5 g (18.3.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide are added. The reaction medium is left overnight under these conditions and 6.5 g (12.3.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide are then added. After 24 h, the reaction mixture is filtered on Celite® , washed with a 1N aqueous solution of hydrochloric acid and then water and dried over magnesium sulfate. After evaporation under reduced pressure, the residue is purified by chromatography on silica gel using a hexane/ethyl acetate mixture (3/1 v/v) as the eluent. 8.1 g (yield:41%) of the expected product are obtained by crystallization from ethanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246961
출처 데이터셋uspto-grants-1993_09
ORD IDord-4b2ec04873ae4d519d8ca8b0c0b1965c
출처 메모uspto-grants-1993_09