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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988597Generated: November 3, 2026

Methyl 1-benzylpyrrolidine-3-carboxylate → (1-Benzylpyrrolidin-3-yl)methanol

https://huagongshe.com/reaction/988597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 1-benzylpyrrolidine-3-carboxylateHCID 4610751—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(1-Benzylpyrrolidin-3-yl)methanolHCID 517665488.8%

Reaction Steps

To a mixture of methyl 1-benzylpyrrolidine-3-carboxylate (11.67 g, 50 mmol) and tetrahydrofuran, at 0° C. was added lithium aluminum hydride (3.795 g, 100 mmol). The reaction was warmed to room temperature and refluxed for 24 hours. After cooling to 0° C., the reaction was quenched with saturated sodium sulfate and warmed to room temperature. Tetrahyrofuran (50 mL) and solid sodium sulfate were added to the mixture. After stirring for 1 hour, the mixture was filtered and the filtrate was concentrated and vacuum dried for 3 days to give the title compound as a colorless oil (8.49 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06635657B1
Source datasetuspto-grants-2003_10
ORD IDord-7fc021bc7cd244c09fe7d87b6a1b1ecd
Source noteuspto-grants-2003_10