HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725111Generated: November 1, 2026
Hydrochloric Acid → HCID 178481746, compound
https://huagongshe.com/reaction/1725111
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 3,5-Dinitrobenzoyl chloride | HCID 7432 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium ethyl malonate | HCID 3446434 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178481746 | HCID 178481746 | 31.8% |
Reaction Steps
Potassium ethyl malonate (11.0 g (0.07 mol)) was suspended in 100 mL of ethyl acetate, and 14.5 g (0.19 mol) of triethylamine and 6.9 g (0.08 mol) of magnesium chloride were sequentially added thereto with stirring under ice cooling. The resulting suspension liquid was stirred at 40° C. for 6 hours and again ice-cooled, and 11.5 g (0.05 mol) of 3,5-dinitrobenzoyl chloride was added dropwise thereto over 1 hour while keeping the reaction solution at 10° C. or less. After the dropwise addition, the stirring was continued at room temperature for 12 hours. Subsequently, 100 mL of 5% hydrochloric acid was added dropwise to the reaction solution, and the organic layer was separated. The obtained organic layer was washed twice with 50 mL of water and then with 30 mL of saturated brine, and the solvent was removed by distillation under reduced pressure. To the residue obtained by the concentration, 100 mL of ethanol was added, and 2.4 g (0.05 mol) of 97% methylhydrazine was then added dropwise at room temperature with stirring. After the dropwise addition, the solution was stirred at room temperature for 1 hour and subsequently at 80° C. for 3 hours. When the reaction was completed, the reaction solution was cooled to room temperature, 300 mL of water was added, and the produced crystal was collected by filtration. The crystal was washed twice with 50 mL of water, and the obtained crystal was recrystallized from 50% aqueous ethanol and dried by a hot air drier to obtain 4.2 g (yield: 30.2%) of the title compound as a red crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07488831B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-71290df1b59645cda0c440f8cddd5925 |
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| Source note | uspto-grants-2009_02 |
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