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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336072Generated: October 30, 2026

Propylenediamine → HCID 57543611, compound

https://huagongshe.com/reaction/336072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylenediamineHCID 6567—
Reactant1,2-bis[4-(trifluoromethyl)phenyl]ethane-1,2-dioneHCID 599378—
SolventEthanolHCID 702—
ProductHCID 57543611HCID 5754361187%

Reaction Steps

First, with 150 mL of dehydrated ethanol as a solvent, 5.07 g of 4,4′-bis(trifluoromethyl)benzil and 1.09 g of 1,2-diaminopropane were mixed, and the mixture was refluxed in a nitrogen atmosphere for four hours. After reaction, a reaction solution was condensed under reduced pressure, and an obtained residue was recrystallized by using ethanol to obtain 2-methyl-5,6-bis(4-trifluoromethylphenyl)-2,3-dihydropyrazine (light yellow crystal, yield: 87%). Further, with 100 mL of dehydrated ethanol as a solvent, 5.05 g of 2-methyl-5,6-bis(4-trifluoromethylphenyl)-2,3-dihydropyrazine that is obtained as described above and 4.26 g of iron (III) chloride were mixed, and the mixture was heated in a nitrogen atmosphere for two hours in a gentle manner. After reaction, water was added into a reaction solution for dilution, and extraction was performed with ether. An extraction solution was dried with magnesium sulfate and filtered, and solvent of filtrate was removed. An obtained residue was recrystallized with ethanol to obtain 5-methyl-2,3-bis(4-trifluoromethylphenyl)pyrazine (CF3DPPR-Me) that is a ligand (white powder, yield: 52%). A synthesis scheme (h-1) relating to the synthesis of Step 1 is shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889266B2
Source datasetuspto-grants-2014_11
ORD IDord-20505feea1a14460b24262a0134caf61
Source noteuspto-grants-2014_11