HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339017Generated: October 29, 2026
Aluminium lithium hydride → Tert-butyl 1-benzyl-3-(hydroxymethyl)pyrrolidin-3-ylcarbamate
https://huagongshe.com/reaction/339017
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 70983305 | HCID 70983305 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 1-benzyl-3-(hydroxymethyl)pyrrolidin-3-ylcarbamate | HCID 10913806 | 56.3% |
Reaction Steps
To a solution of methyl 1-benzyl-3-(tert-butoxycarbonylamino)pyrrolidine-3-carboxylate (21.7 g, 64.9 mmol) in THF (320 mL) was added dropwise a solution of LiAlH4 in THF (1.0 M, 55.2 mL, 55.2 mmol) at −78° C. under nitrogen. The reaction mixture was warmed to 0° C. for 5 minutes and then quenched by dropwise addition of water (2.1 mL) followed by 15% NaOH (2.1 mL) and water (6.3 mL). The reaction mixture was stirred at ambient temperature for 15 minutes and then filtered through Celite®. The filtrate was concentrated under reduced pressure and purified by flash chromatography on silica gel (4% MeOH in DCM) to give tert-butyl 1-benzyl-3-(hydroxymethyl)pyrrolidin-3-ylcarbamate (11.2 g, 56%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889704B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-ac6a51f66c304c0098aa46e668e4e475 |
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| Source note | uspto-grants-2014_11 |
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