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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263891Generated: October 26, 2026

Methanol → 2,5,6-Trichloro-1-(beta-D-arabinofuranosyl)benzimidazole

https://huagongshe.com/reaction/263891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium HydroxideHCID 14923—
ReactantBoron TrichlorideHCID 25135—
Reactant2,5,6-Trichloro-1-(2,3,5-tri-O-benzyl-beta-D-arabinofuranosyl)benzimidazoleHCID 53992940—
SolventDichloromethaneHCID 6344—
Product2,5,6-Trichloro-1-(beta-D-arabinofuranosyl)benzimidazoleHCID 53698358—

Reaction Steps

Compound 133 (1.25 g 2 mmole) was dissolved in dry CH2Cl2 (20 ml) and this solution was cooled in an acetone-dry ice bath. A 1M solution of BCl3 in CH2Cl2 (10 ml) was added and the mixture was stirred at -70° for 4.5 hr. At this point TLC showed no starting material. CH3OH (10 ml) was added and the solution was made neutral with NH4OH. The solution was evaporated in vacuo to dryness. H2O (20 ml) was added and the solution was extracted with EtOAc. The EtOAc layer was washed with H2O, dried (Na2SO4) and evaporated in vacuo to obtain a syrup. This syrup was subjected to flash column chromatography on silica gel (Kieselgel 60, 230-400 mesh) with CH2Cl--MeOH (20:1) as eluent solvent to give 134. Yield 0.551 g, 77.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646125
Source datasetuspto-grants-1997_07
ORD IDord-50b963f64b68477098af92a6185dd1af
Source noteuspto-grants-1997_07