돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6043생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/6043

반응식

참여 물질

역할이름HCID투입량
반응물3-CyanophenolHCID 13394—
반응물2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
촉매ZincchlorideHCID 3007855—
촉매Silver imidazolateHCID 10931941—
용매DichloromethaneHCID 6344—
생성물3-cyanophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranosideHCID 1506785633.3%

반응 단계

If the procedure described in Preparation LXXXIII is followed starting from 2 g (16.8.10-3 mol) of 3-hydroxybenzonitrile, 2.9 mg (16.5.10-3 mol) of silver imidazolate, 6.5 g (18.3.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide and 4.6 g (33.6.10-3 mol) of zinc chloride in 80 ml of methylene chloride, 2.2 g (yield: 33%) of the expected product are obtained after purification by chromatography on silica gel using a hexane/ethyl acetate mixture (3/1 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-9094a061a11242d6a707afb2325720a6
출처 메모uspto-grants-1993_09