HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzonitrile → 1-Phenyl-cyclopropylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | HCID 178461630 | HCID 178461630 | — |
| Catalyst | HCID 178460666 | HCID 178460666 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Phenyl-cyclopropylamine | HCID 194549 | 31.5% |
Reaction Steps
To benzonitrile (1.03 g, 10 mmol) in ether (50 ml) at −70° C. was added Ti(OiPr)4 (3.22 ml, 11 mmol) and EtMgBr (3M in ether, 7.34 mL, 22 mmol) dropwise, the resulting yellow suspension was warmed up to room temperature over 1 h. After stirring for additional 30 min, the dark brown solution was added BF3.Et2O (2.47 mL, 20 mL) at room temperature. The mixture was further stirred for 1 h, and was quenched by 1N HCl (30 mL) and 5N NaOH (30 mL), the suspension was extracted with ether, ether layer was combined, concentrated to give crude residue, which was purified by column (Hexanes/EtOAc, 2:1 to 1:9) to give 1-phenylcyclopropanamine (420 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367689B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-823b6ae9ef4b4d1da721d56cc0e4d230 |
| Source note | uspto-grants-2013_02 |