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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473999Generated: November 3, 2026

Hydrochloric Acid → N-tert-butyl-1-benzhydryl-3-methylazetidin-3-amine hydrochloride

https://huagongshe.com/reaction/473999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-ButylamineHCID 6385—
Reactant1-Benzhydryl-3-methylazetidin-3-yl methanesulfonateHCID 10065295—
SolventDiethyl EtherHCID 3283—
SolventIsopropanolHCID 3776—
ProductN-tert-butyl-1-benzhydryl-3-methylazetidin-3-amine hydrochlorideHCID 6845765074%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-benzhydryl-3-methylazetidin-3-yl methanesulfonate (2.00 g, 6.23 mmol) in iso-propanol (10 ml) was added tert-butyl amine (1.36 g, 18.63 mmol). The mixture was heated at 80° C. for 3 h. The reaction mixture was then allowed to cool to room temperature and concentrated. The residue was slurried with ethyl acetate and filtered, washing with further ethyl acetate and then concentrated to give a solid. The solid was slurried in ether and hydrochloric acid (20 ml, 2M in ether) was added, then stirred for 10 mins and filtered to provide the title compound as a tan solid (1.69 g, 74%). 1H NMR (DMSO) 1.40 (9H, s), 1.99 (3H, s), 3.85 (2H, brs), 4.11 (2H, brs), 4.71 (1H, brs), 7.35-7.50 (6H, m), 7.70-7.81 (4H, m), 10.23 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637511B2
Source datasetuspto-grants-2014_01
ORD IDord-6f201b58f4dd44f8aff34c55cb9a9437
Source noteuspto-grants-2014_01