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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732660Generated: October 31, 2026

Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylate → (1-Benzylpyrrolidin-3-yl)methanol

https://huagongshe.com/reaction/732660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 1-benzyl-5-oxopyrrolidine-3-carboxylateHCID 98909—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(1-Benzylpyrrolidin-3-yl)methanolHCID 5176654—

Reaction Conditions

Temperature60 °C

Reaction Steps

In accordance with the technique of “Bioorganic and Medicinal Chemistry Letters”, 1991, vol. 1, no. 12, p. 757-760, methyl 1-benzyl-5-oxopyrrolidine-3-carboxylate (mfd. by Aldrich, USA) was added to a THF solution of lithium aluminum hydride in an ice bath, and then stirred at 60° C. for 1.5Hours. Thereafter, its work-up and purification were carried out in the standard method to obtain (1-benzylpyrrolidin-3-yl)methanol. FP: 192.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585886B2
Source datasetuspto-grants-2009_09
ORD IDord-5590880cad1e4b0f87d032fc64e29eb9
Source noteuspto-grants-2009_09