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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6011생성일: 2026년 10월 25일

Mercuric cyanide → 3,4,5-trimethoxyphenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranoside

https://huagongshe.com/reaction/6011

반응식

참여 물질

역할이름HCID투입량
반응물Mercuric cyanideHCID 11591—
반응물2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
반응물3,4,5-TrimethoxybenzenethiolHCID 15198240—
생성물3,4,5-trimethoxyphenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranosideHCID 1479535128%

반응 단계

If the procedure described in Preparation I is followed starting from 11.35 g (57.10-3 mol) of 3,4,5-trimethoxybenzenethiol, 14.32 g (57.10-3 mol) of mercuric cyanide, Hg(CN)2, and 22.15 g (62.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide, 7.52 g (yield: 28%) of the expected product are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246961
출처 데이터셋uspto-grants-1993_09
ORD IDord-a168521407ce43298f3e0fd66fa637a9
출처 메모uspto-grants-1993_09