HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957787Generated: November 1, 2026
Ethylenediamine → N-[3,5-bis(trifluoromethyl)benzyl]ethylenediamine
https://huagongshe.com/reaction/1957787
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | [3,5-Bis(trifluoromethyl)phenyl]methyl methanesulfonate | HCID 18387265 | — |
| Reactant | 2-Chloro-4-phenylnicotinic acid | HCID 18387312 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3,5-bis(trifluoromethyl)benzyl]ethylenediamine | HCID 18387337 | — |
Reaction Steps
Thionyl chloride (0.15 ml) and DMF (catalytic amount) were added to a THF (5 ml) solution of 2-chloro-4-phenyl-3-pyridinecarboxylic acid (145 mg) and heated under reflux for 2 hours. The solvent was removed by distillation, and the residue was dissolved in THF (5 ml). The resulting solution was added to a mixture of N-[3,5-bis(trifluoromethyl)benzyl]-N'-tert-butoxycarbonylethylenediamine (240 mg), triethylamine (0.26 ml) and THF (10 ml), while cooling with ice, and stirred for 3 hours at room temperature. The N-[3,5-bis (trifluoromethyl)benzyl]-N'-tert-butoxycarbonylethylenediamine used herein was prepared as an oily compound, by reacting ethylenediamine with 3,5-bis(trifluoromethyl)benzyl methanesulfonate in THF to give an oily compound of N- [3,5-bis (trifluoromethyl)benzyl]ethylenediamine, followed by further reacting the compound with di-tert-butyl dicarbonate in the presence of triethylamine in THF.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05786352 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-3b40b75ebac442e9a803fcee6be1bae1 |
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| Source note | uspto-grants-1998_07 |
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