HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198604Generated: October 31, 2026
Water → N,N-dimethyl-1-(phenylmethyl)-3-pyrrolidinemethanamine
https://huagongshe.com/reaction/1198604
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N,N-dimethyl-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxamide | HCID 14280891 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N-dimethyl-1-(phenylmethyl)-3-pyrrolidinemethanamine | HCID 14280892 | 58.2% |
Reaction Steps
A solution of 2.91 g (11.8 mmol) N,N-dimethyl-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxamide and 15 mL anhydrous tetrahydrofuran was added dropwise into a suspension of 1.41 g (35 mmol) lithium aluminum hydride in 30 mL tetrahydrofuran. The reaction was refluxed overnight then cooled to room temperature. To the solution was added dropwise successively 1.5 mL water, 1.5 mL 15% sodium hydroxide and 4.5 mL of water. The resulting precipitate was filtered. The filtrate was concentrated under reduced pressure, dissolved in dichloromethane, dried over magnesium sulfate and the solvent evaporated under reduced pressure. The residue was bulb to bulb distilled giving 1.5 g (58%) of N,N-dimethyl-1-(phenylmethyl)-3-pyrrolidinemethanamine as a clear liquid. This material was used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05281612 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-65ef5fb1ccb04479858f3327fc504351 |
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| Source note | uspto-grants-1994_01 |
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