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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1883355Generated: October 25, 2026

Ethylene Glycol → N-benzyl-4-chloroaniline

https://huagongshe.com/reaction/1883355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantBenzylamineHCID 7504—
Reactant1-Chloro-4-iodobenzeneHCID 12510—
ReactantPotassium Phosphate, TribasicHCID 62657—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventIsopropanolHCID 3776—
SolventEthyl acetate hexaneHCID 21226206—
ProductN-benzyl-4-chloroanilineHCID 7628184%

Reaction Steps

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, Rƒ=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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06759554B2
Source datasetuspto-grants-2004_07
ORD IDord-17560122e90c4a2d888730f296111cd3
Source noteuspto-grants-2004_07