Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6011Generated: October 25, 2026

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

https://huagongshe.com/reaction/6011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMercuric cyanideHCID 11591—
Reactant2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
Reactant3,4,5-TrimethoxybenzenethiolHCID 15198240—
Product3,4,5-trimethoxyphenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranosideHCID 1479535128%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246961
Source datasetuspto-grants-1993_09
ORD IDord-a168521407ce43298f3e0fd66fa637a9
Source noteuspto-grants-1993_09