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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1243007Erstellt: 26. Oktober 2026

Ethylene Glycol → N-Benzyl-3,5-dimethylaniline

https://huagongshe.com/reaction/1243007

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktBenzylamineHCID 7504—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt1-Iodo-3,5-dimethylbenzeneHCID 140924—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelEthyl acetate hexaneHCID 21226206—
ProduktN-Benzyl-3,5-dimethylanilineHCID 1017670184%

Reaktionsschritte

The general procedure under argon or air was followed using copper(I) iodide (10 mg, 0.05 mmol), K3PO4 (425 mg, 2.00 mmol), benzylamine (131 μL, 1.20 mmol), 5-iodo-m-xylene (144 μl, 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=20/1, Rf=0.5) afforded 5-(N-benzyl)amino-m-xylene (177 mg, 84% isolated yield) as colorless liquid. The spectral data (1H NMR) matched with the literature references and GC analysis indicated >95% purity. See Wolfe, J. P.; Buchwald, S. L. J. Org. Chem. 2000, 65, 1144–1157.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07115784B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-cd0a782c6e844affa8e4491609cda759
Quellennotizuspto-grants-2006_10