HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254813Generated: October 29, 2026
O-Phenylenediamine → HCID 21459115, compound
https://huagongshe.com/reaction/2254813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | HCID 19000171 | HCID 19000171 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21459115 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05236952 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-d2487007909b4ebdba993d5c062bd46f |
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| Source note | uspto-grants-1993_08 |
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