Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467520Generated: October 25, 2026

Sodium hydride → Benzyl 3-(2-benzyloxyethoxy)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/467520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBenzene, ((2-bromoethoxy)methyl)-HCID 73833—
ReactantBenzyl 3-hydroxypyrrolidine-1-carboxylateHCID 560953—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 3-(2-benzyloxyethoxy)pyrrolidine-1-carboxylateHCID 7092704322.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 1.29 g of benzyl 3-hydroxypyrrolidine-1-carboxylate in 80 ml of THF is cooled to 0° C., 0.245 g of 60% NaH in oil is added and then 1.26 g of [(2-bromoethoxy)methyl]benzene and 0.108 g of tetrabutylammonium iodide and it is heated at 80° C. for 3 hours. 0.28 g of NaH and 0.40 g of [(2-bromoethoxy)methyl]benzene are added and it is heated at 80° C. for 2 hours. The reaction mixture is concentrated under vacuum, the residue is extracted with DCM, the organic phase is washed with 0.1M HCl solution, with a saturated solution of NaHCO3, it is dried and the solvent is evaporated under vacuum. The product thus obtained is purified by preparative HPLC and 0.46 g of the expected compound is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623862B2
Source datasetuspto-grants-2014_01
ORD IDord-31c6ebefc897422a9c8ff8c9e97cc707
Source noteuspto-grants-2014_01