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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341814Generated: October 25, 2026

Ammonium Chloride → 2-(1-Benzhydrylazetidin-3-YL)ethanamine

https://huagongshe.com/reaction/341814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHydrideHCID 166653—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3-Cyanomethyl-1-benzhydryl azetidineHCID 22257633—
SolventTetrahydrofuranHCID 8028—
Product2-(1-Benzhydrylazetidin-3-YL)ethanamineHCID 2225763487%

Reaction Steps

5.7 g (21.7 mmol) of 3-cyanomethyl-1-benzhydryl azetidine was added slowly to a suspention of 2.9 g (76.0 mmol) of LiAlH4 in 80 mL of dry THF at roomtemperature. The reaction mixture was refluxed for 4 h. Excess hydride reagent was hydrolyzed by careful addition, with cooling, of NH4Cl(aq), the gelatinous mixture was filtered and the filter cake was washed repeatedly with THF. The solvent was evaporated, the residue was dissolved in diethyl ether, washed with brine and dried with Na2SO4. Evaporation of the solvent gave 5.0 g (87%) of the title compound. p (vi) 3-(N-tert-butyloxycarbonylaminoethyl)-1-benzhydryl azetidine

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856307
Source datasetuspto-grants-1999_01
ORD IDord-41b119b7bc4141bebcfa20f0a74c93fc
Source noteuspto-grants-1999_01