HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499071Generated: October 30, 2026
Hydrochloric Acid → N-tert-butyl-1-benzhydryl-3-methylazetidin-3-amine hydrochloride
https://huagongshe.com/reaction/499071
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 1-Benzhydryl-3-methylazetidin-3-yl methanesulfonate | HCID 10065295 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | N-tert-butyl-1-benzhydryl-3-methylazetidin-3-amine hydrochloride | HCID 68457650 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767672B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-e4b12d375e1b44638b15b7c8a4dcec43 |
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| Source note | uspto-grants-2010_08 |
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