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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448668Generated: October 29, 2026

2-o-Acetyl-3,5-bis-o-(2,4-dichlorobenzyl)-1-o-methyl-alpha-d-ribofuranose → 1-Methyl-3,5-bis-O-(2,4-dichlorobenzyl)-alpha-D-ribofuranoside

https://huagongshe.com/reaction/448668

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-o-Acetyl-3,5-bis-o-(2,4-dichlorobenzyl)-1-o-methyl-alpha-d-ribofuranoseHCID 11016814—
SolventPotassium CarbonateHCID 11430—
Product1-Methyl-3,5-bis-O-(2,4-dichlorobenzyl)-alpha-D-ribofuranosideHCID 10994483101.6%

Reaction Steps

A mixture of 2-O-acetyl-3,5-bis-O-(2,4-dichlorophenylmethyl)-1-O-methyl-α-D-ribofuranose [for preparation, see: Helv. Chim. Acta 78: 486 (1995)] (52.4 g, 0.10 mol) in methanolic K2CO3 (500 mL, saturated at room temperature) was stirred at room temperature for 45 min. and then concentrated under reduced pressure. The oily residue was suspended in CH2Cl2 (500 mL), washed with water (300 mL+5×200 mL) and brine (200 mL), dried (Na2SO4), filtered, and concentrated to give the title compound (49.0 g) as colorless oil, which was used without further purification in Step B below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481712B2
Source datasetuspto-grants-2013_07
ORD IDord-325e74754bb041eaa601b7d704aa95e3
Source noteuspto-grants-2013_07