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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021225Generated: November 1, 2026

Benzyl Bromide → 3-(Phenylmethoxy)azetidine

https://huagongshe.com/reaction/1021225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3-(Phenylmethoxy)azetidineHCID 25220690—

Reaction Steps

tert-Butyl 3-hydroxyazetidine-1-carboxylate (3.0 g) was mixed with THF (30 ml), and sodium hydride (55% suspended in oil) (600 mg) was added thereto, followed by stirring at room temperature for 10 minutes. Benzyl bromide (2.5 ml) was added thereto, followed by stirring at room temperature for 3 hours. Water and EtOAc were added to the reaction mixture, and the organic layer was dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was mixed with DCE (30 ml), and TFA (15 g) was added thereto, followed by stirring at room temperature for 3 hours. The reaction mixture was concentrated under reduced pressure and purified by basic silica gel column chromatography (CHCl3/MeOH) to obtain 3-(benzyloxy)azetidine (2.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716470B2
Source datasetuspto-grants-2014_05
ORD IDord-2ab5bf51c305450fa0e7c63f01bf182f
Source noteuspto-grants-2014_05