Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6046Generated: October 27, 2026

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

https://huagongshe.com/reaction/6046

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrophenolHCID 6947—
Reactant2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
CatalystZincchlorideHCID 3007855—
CatalystSilver imidazolateHCID 10931941—
SolventDichloromethaneHCID 6344—
Product2-nitrophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranosideHCID 1506785815.3%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246961
Source datasetuspto-grants-1993_09
ORD IDord-06ef2526ca4b4e82962cc682dc5f8a8a
Source noteuspto-grants-1993_09