HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527521Generated: November 2, 2026
Boron trifluoride etherate → 1-(3-Chlorophenyl)cyclopropanamine
https://huagongshe.com/reaction/1527521
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Benzonitrile, m-chloro- | HCID 13015 | — |
| Reactant | HCID 178461633 | HCID 178461633 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(3-Chlorophenyl)cyclopropanamine | HCID 11084270 | — |
Reaction Steps
To a solution of 3-chlorobenzonitrile (1 g, 7.27 mmol) and titanium (IV) isopropoxide (2.34 mL, 8 mmol) in Et2O (35 mL) at −78° C. was added ethyl magnesium chloride in THF (5.71 mL, 15.99 mmol). The solution was stirred for 10 min at −78° C. then at 25° C. for 1 h. BF3.Et2O (1.82 mL, 14.54 mmol) was added and the solution was stirred for 1 h at 25° C. The reaction mixture was quenched with 1N HCl (22 mL) Et2O was added (100 mL). Then 10% aq. NaOH (70 mL) was added and the layers were separated. The organic layer was dried over Na2SO4, filtered and concentrated. The crude residue was purified by preparative HPLC (Waters SunFire C18-ODB, 5 μm, 19×50 mm, 5% CH3CN/H2O 2.5 min, 5-100% CH3CN/H2O in 10 min, CH3CN/H2O containing 0.1% HCOOH flow: 20 mL/min) to give after lyophilization of the purified fractions the title compound. MS (UPLC-MS): 170 [M+H]+, 168 [M−H]−; tR (HPLC conditions f): 1.22 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085555B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-0d821cb87d224c9381604e6e662de211 |
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| Source note | uspto-grants-2015_07 |
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