HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158310Generated: October 29, 2026
Hydrochloric Acid → HCID 178526717, compound
https://huagongshe.com/reaction/1158310
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-(2-Cyanoethyl)-4-nitro-2-(4-nitrophenylthio)imidazole | HCID 23080246 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178526717 | HCID 178526717 | 58% |
Reaction Steps
To tetrahydrofuran (1 ml) solution of 1-(2-cyanoethyl)-4-nitro-2-(4-nitrophenylthio)imidazole (27 mg) was added 1,8-diazabicyclo[5.4.0]undecene-7 (0.02 ml) at a room temperature, and stirred at the same temperature for 3 hours. To the reaction mixture were added 1N hydrochloric acid (0.7 ml), water and ethyl acetate, then the organic layer was taken by liquid separation. The ethyl acetate layer was washed with water and an aqueous solution being saturated with sodium chloride, then dried over anhydrous sodium sulfate. The residue obtained by removal of the solvent by distillation was purified by use of a thin layer chromatography (eluent: dichloromethane/ethyl acetate=9/1), there was obtained 4-nitro-2-(4-nitrophenylthio)imidazole (13 mg, yield 58%) as reddish brown powdery product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807843B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-03736562dfe94b90aa52b31724492c7b |
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| Source note | uspto-grants-2010_10 |
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