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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781902Generated: October 30, 2026

O-Phenylenediamine → HCID 21459115, compound

https://huagongshe.com/reaction/1781902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
ReactantHCID 19000171HCID 19000171—
SolventEthanolHCID 702—
ProductHCID 21459115HCID 21459115—

Reaction Steps

19.7 g of ethyl (3,4-dimethoxy-5-nitrophenyl)hydroxyacetimidate are dissolved in 500 ml of ethanol. 6.73 g of o-phenylenediamine are added, the mixture is stirred at room temperature for 2 hours and subsequently held at the reflux temperature overnight. After distillation of the solvent, the residue is treated with 50 ml of water, made alkaline with sodium carbonate solution and extracted twice with 250 ml of methylene chloride each time. The organic phase is washed with water, dried over sodium sulfate and evaporated. The orange residue obtained is chromatographed on 400 g of silica gel with methylene chloride/ethyl acetate (1:1). From ether/hexane there is obtained α-(3,4-dimethoxy-5-nitrophenyl)-2-benzimidazolemethanol in the form of yellowish crystals of m.p. 50° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633371
Source datasetuspto-grants-1997_05
ORD IDord-030e0caa3c5b4b03bb432d63d84e972a
Source noteuspto-grants-1997_05