HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620850Generated: October 27, 2026
Water → [(1-Benzylpyrrolidin-3-yl)methyl](2,2,2-trifluoroethyl)amine
https://huagongshe.com/reaction/620850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-benzyl-5-oxo-N-(2,2,2-trifluoroethyl)pyrrolidine-3-carboxamide | HCID 13491796 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [(1-Benzylpyrrolidin-3-yl)methyl](2,2,2-trifluoroethyl)amine | HCID 14280884 | 0.1% |
Reaction Steps
A mixture of 8.50 g (28.3 mole) of 5-oxo-1-(phenylmethyl)-N-(2,2,2-trifluoroethyl)-3-pyrrolidinecarboxamide in 100 ml tetrahydrofuran was added dropwise to 3.22 g (84.9 mmole) of lithium aluminum hydride in 50 ml tetrahydrofuran. The reaction was refluxed two hours, then stirred at room temperature overnight. The reaction was cooled in an ice bath and 3.2 ml of water, 3.2 ml of 15% sodium hydroxide, and 9.6 ml of water were added. The precipitated salts were filtered and washed with hot ethanol. The combined filtrates were concentrated under reduced pressure. The residue was taken up in dichloromethane, filtered, and dried over magnesium sulfate. The solvent was removed at reduced pressure to give 7.15 g of 1-(phenylmethyl)-N-(2,2,2-trifluoroethyl)-3-pyrrolidinemethanamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04822801 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-0d95285ff9534bf39d2b4e4093cff447 |
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| Source note | uspto-grants-1989_04 |
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