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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511736Generated: October 31, 2026

Hydrochloric Acid → HCID 86693872, compound

https://huagongshe.com/reaction/511736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN,N-DimethylanilineHCID 949—
Reactant2,6-DimethylanilineHCID 6896—
ReactantHCID 86693871HCID 86693871—
SolventDichloromethaneHCID 6344—
ProductHCID 86693872HCID 8669387231%

Reaction Conditions

Temperature120 °C

Reaction Steps

First, 12.6 g (43.3 mmol) of N-[1-chloro-1-(2-methylphenyl)methylidene]-N′-[1-chloro-(1-phenyl)methylidene]hydrazine, 15.7 g (134.5 mmol) of 2,6-dimethylaniline, and 100 ml of N,N-dimethylaniline were put into a 500-ml recovery flask and heated and stirred at 120° C. for 20 hours. After reaction for the predetermined time, this reacted solution was slowly added to 200 ml of 1N hydrochloric acid. Dichloromethane was added to this solution and an objective substance was extracted to an organic layer. The obtained organic layer was washed with water and an aqueous solution of sodium hydrogen carbonate, and was dried with magnesium sulfate. The magnesium sulfate was removed by gravity filtration, and the obtained filtrate was concentrated to give a black liquid. This liquid was purified by silica gel column chromatography. A mixed solvent of ethyl acetate and hexane in a ratio of 1:5 was used as a developing solvent. The obtained fraction was concentrated to give a white solid. This solid was recrystallized with ethyl acetate to give 4.5 g of a white solid of Hmpptz-dmp in a yield of 31%. A synthesis scheme of Step 1 is shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09099617B2
Source datasetuspto-grants-2015_08
ORD IDord-e2e6aece3b3e40739bbd35f5c04288b4
Source noteuspto-grants-2015_08