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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6034생성일: 2026년 10월 23일

4-Nitrophenol → 4-nitrophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranoside

https://huagongshe.com/ko/reaction/6034

반응식

참여 물질

역할이름HCID투입량
반응물4-NitrophenolHCID 980—
반응물2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
촉매ZincchlorideHCID 3007855—
촉매Silver imidazolateHCID 10931941—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물4-nitrophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranosideHCID 1506784825.2%

반응 조건

온도50 °C

반응 단계

A suspension of 5.6 g (15.8.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide, 2 g (14.3.10-3 mol) of 4-nitrophenol, 4 g (29.3.10-3 mol) of zinc chloride and 3.8 g (21.7.10-3 mol) of silver imidazolate in 80 ml of anhydrous methylene chloride is stirred at 50° C., under an inert atmosphere, in the absence of light and in the presence of a molecular sieve (400 pm). After 48 h at this temperature, the reaction mixture is filtered on Celite®, washed with a 1N aqueous solution of hydrochloric acid, then a 1N solution of sodium hydroxide and finally water and dried over magnesium sulfate (MgSO4). After evaporation to dryness, the residue is purified by chromatography on silica gel using a hexane/ethyl acetate mixture (3/1 v/v) as the eluent. 1.5 g (yield: 25%) of the expected product are obtained by precipitation in ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246961
출처 데이터셋uspto-grants-1993_09
ORD IDord-b9a267834ffc4d2eb782eaa76b1e6127
출처 메모uspto-grants-1993_09