HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440110Generated: November 1, 2026
Water → 4-Amino-1-(phenylmethyl)-3-pyrrolidinemethanol
https://huagongshe.com/reaction/1440110
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium bis(2-methoxyethoxy)aluminiumhydride | HCID 21584525 | — |
| Reactant | HCID 86745294 | HCID 86745294 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Amino-1-(phenylmethyl)-3-pyrrolidinemethanol | HCID 15023851 | 52.4% |
Reaction Steps
A solution of 5.24 g (0.02 mole) of 1-benzyl-3-ethoxycarbonyl-4-hydroxyiminopyrrolidine [prepared as described in step (a) above] in 10 ml of toluene was added dropwise to 28 ml of a 3.4M solution of sodium bis(2-methoxyethoxy)aluminum hydride in toluene over a period of 1 hour. The mixture was stirred at room temperature for 1.5 hours and was then heated under reflux for 2 hours. At the end of this time, the reaction mixture was allowed to cool to room temperature, after which ice and water were added to it to form a precipitate, which was removed by filtration. The filtrate was concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel using methanol as the eluent, to afford 2.16 g of 3-amino-1-benzyl-4-hydroxymethylpyrrolidine as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05496951 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-f068676bc58140c3b5a8a2811ab70e35 |
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| Source note | uspto-grants-1996_03 |
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