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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725111Generated: November 1, 2026

Hydrochloric Acid → HCID 178481746, compound

https://huagongshe.com/reaction/1725111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethylhydrazineHCID 6061—
Reactant3,5-Dinitrobenzoyl chlorideHCID 7432—
ReactantTriethylamineHCID 8471—
ReactantPotassium ethyl malonateHCID 3446434—
ReactantMagnesium ChlorideHCID 5360315—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 178481746HCID 17848174631.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488831B2
Source datasetuspto-grants-2009_02
ORD IDord-71290df1b59645cda0c440f8cddd5925
Source noteuspto-grants-2009_02