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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384268Generated: October 25, 2026

Benzonitrile → 1-Phenyl-cyclopropylamine

https://huagongshe.com/reaction/384268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrileHCID 7505—
ReactantBoron trifluoride etherateHCID 8000—
ReactantHCID 178461630HCID 178461630—
CatalystHCID 178460666HCID 178460666—
SolventDiethyl EtherHCID 3283—
Product1-Phenyl-cyclopropylamineHCID 19454931.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367689B2
Source datasetuspto-grants-2013_02
ORD IDord-823b6ae9ef4b4d1da721d56cc0e4d230
Source noteuspto-grants-2013_02