HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 2-(1-Benzhydrylazetidin-3-YL)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Hydride | HCID 166653 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 3-Cyanomethyl-1-benzhydryl azetidine | HCID 22257633 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(1-Benzhydrylazetidin-3-YL)ethanamine | HCID 22257634 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05856307 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-41b119b7bc4141bebcfa20f0a74c93fc |
| Source note | uspto-grants-1999_01 |