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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6046생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/6046

반응식

참여 물질

역할이름HCID투입량
반응물2-NitrophenolHCID 6947—
반응물2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
촉매ZincchlorideHCID 3007855—
촉매Silver imidazolateHCID 10931941—
용매DichloromethaneHCID 6344—
생성물2-nitrophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranosideHCID 1506785815.3%

반응 단계

If the procedure described in Preparation LXXXIII is followed starting from 2 g (14.4.10-3 mol) of 2-nitrophenol, 2.5 g (14.2.10-3 mol) of silver imidazolate, 6 g (15.7.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide and 4 g (29.3.10-3 mol) of zinc chloride in 80 ml of methylene chloride, 0.91 g (yield: 15%) of the expected product is obtained after purification by chromatography on silica gel using a hexane/ethyl acetate mixture (2/1 v/v) as the eluent, and precipitation in ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246961
출처 데이터셋uspto-grants-1993_09
ORD IDord-06ef2526ca4b4e82962cc682dc5f8a8a
출처 메모uspto-grants-1993_09