HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336072Generated: October 30, 2026
Propylenediamine → HCID 57543611, compound
https://huagongshe.com/reaction/336072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylenediamine | HCID 6567 | — |
| Reactant | 1,2-bis[4-(trifluoromethyl)phenyl]ethane-1,2-dione | HCID 599378 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57543611 | HCID 57543611 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889266B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-20505feea1a14460b24262a0134caf61 |
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| Source note | uspto-grants-2014_11 |
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