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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 984592Erstellt: 24. Oktober 2026

Ethylene Glycol → N-benzyl-4-chloroaniline

https://huagongshe.com/de/reaction/984592

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktBenzylamineHCID 7504—
Edukt1-Chloro-4-iodobenzeneHCID 12510—
EduktPotassium Phosphate, TribasicHCID 62657—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelEthyl acetate hexaneHCID 21226206—
ProduktN-benzyl-4-chloroanilineHCID 7628184%

Reaktionsschritte

The general procedure under argon was followed using copper(I) iodide (10 mg, 0.05 mmol), K3PO4 (425 mg, 2.00 mmol), benzylamine (131 μL, 1.20 mmol), 4-chloroiodobenzene (239 mg, 1.00 mmol), ethylene glycol (111 μL, 2.00 mmol) and 2-propanol (1.0 mL). Column chromatography using a solvent mixture (hexane/ethyl acetate=10/1, Rf=0.4) afforded N-(4-chlorophenyl)benzylamine (182 mg, 84% isolated yield) as light yellow liquid. The spectral data (1H NMR) matched with the literature references and GC analysis indicated >95% purity. See Burton, R. D.; Bartberger, M. D.; Zhang, Y.; Eyler, J. R.; Schanze, K. S. J. Am. Chem. Soc. 1996, 118, 5655-5664.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06867298B2
Quelldatensatzuspto-grants-2005_03
ORD IDord-7b92859995b6480895a77d0ef477857d
Quellennotizuspto-grants-2005_03