HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243020Generated: October 30, 2026
Ethylene Glycol → Ethyl 4-(benzylamino)benzoate
https://huagongshe.com/reaction/1243020
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Ethyl 4-iodobenzoate | HCID 142891 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | Ethyl 4-(benzylamino)benzoate | HCID 3832836 | 50% |
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), ethyl 4-iodobenzoate (167 μl, 1.00 mmol), ethylene glycol (111 μL, 2.00 mmol) and ethanol (1.0 mL). Column chromatography using a solvent mixture (hexane/ethyl acetate=5/1, Rf=0.4) afforded ethyl 4-(N-benzyl)aminobenzoate (113 mg, 50% isolated yield) as light yellow solid. The spectral data (1H NMR) matched with the literature references and GC analysis indicated >95% purity. See Albright, J. D.; DeVries, V. G.; Largis, E. E.; Miner, T. G. Reich, M. F.; Schaffer, S.; Shepherd, R. G.; Upeslacis, J. J. Med. Chem. 1983, 26, 1378–1393; and Onaka, M.; Umezono, A.; Kawai, M.; Izumi, Y. J. Chem. Soc., Chem. Commun. 1985, 1202–1203.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07115784B2 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-6725b6075fdb480895fe2f294197cb0e |
|---|
| Source note | uspto-grants-2006_10 |
|---|