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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 384268Erstellt: 24. Oktober 2026

Benzonitrile → 1-Phenyl-cyclopropylamine

https://huagongshe.com/de/reaction/384268

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzonitrileHCID 7505—
EduktBoron trifluoride etherateHCID 8000—
EduktHCID 178461630HCID 178461630—
KatalysatorHCID 178460666HCID 178460666—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1-Phenyl-cyclopropylamineHCID 19454931,5%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367689B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-823b6ae9ef4b4d1da721d56cc0e4d230
Quellennotizuspto-grants-2013_02