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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantTetrahydrofuranHCID 8028—
ReactantBenzonitrile, m-chloro-HCID 13015—
ReactantHCID 178461633HCID 178461633—
CatalystTitanium isopropoxideHCID 11026—
SolventDiethyl EtherHCID 3283—
Product1-(3-Chlorophenyl)cyclopropanamineHCID 11084270—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-0d821cb87d224c9381604e6e662de211
Source noteuspto-grants-2015_07