HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → 1-(Tetrahydro-2H-pyran-4-YL)cyclopropanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Oxane-4-carbonitrile | HCID 11815837 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(Tetrahydro-2H-pyran-4-YL)cyclopropanamine | HCID 57790295 | 66.9% |
Reaction Steps
Combined tetrahydro-2H-pyran-4-carbonitrile (1.000 g, 9.00 mmol) and titanium (IV)isopropoxide (2.90 mL, 9.90 mmol) in ether (45.0 mL), then ethylmagnesium bromide (6.60 mL, 19.79 mmol) was added and the reaction was allowed to warm to room temperature for 1 hour. The reaction was stirred for an additional 30 minutes and boron trifluoride etherate (2.280 mL, 18.0 mmol) was added and the reaction was stirred for 2 hours. The reaction was then diluted with 10 mL water and 20 mL 1 N HCl and extracted twice with 200 mL EtOAc. The organic layers were combined and concentrated to afford the title compound (850 mg, 53.5%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09345713B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-324d2f9cefc24e0f85048728a9e810eb |
| Source note | uspto-grants-2016_05 |