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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 600998Erstellt: 25. Oktober 2026

Ethylene Glycol → 4-(3-Iodophenyl)morpholine

https://huagongshe.com/reaction/600998

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktMorpholineHCID 8083—
EduktBenzene, 1,3-diiodo-HCID 12270—
EduktPotassium Phosphate, TribasicHCID 62657—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelIsopropanolHCID 3776—
Produkt4-(3-Iodophenyl)morpholineHCID 5453643441%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of 1,3-diiodobenzene (5.05 g, 15.3 mmol) in isopropanol (16 mL) under nitrogen was added morpholine (1.33 g, 1.33 mL, 15.3 mmol), potassium phosphate (6.50 g, 30.6 mmol), ethylene glycol (1.90 g, 1.70 mL, 30.6 mmol) and copper (I) iodide (146 mg, 0.765 mmol). The mixture was heated at 80° C. for 15 h, and then cooled to room temperature. The solids were removed by filtration and the solution was concentrated. The residue was purified by silica gel column chromatograghy eluted with EtOAc:hexanes (5 to 25% EtOAc) to give 4-(3-iodo-phenyl)-morpholine (1.81 g, 41%) as a colorless oil. MS (ES+): m/z=290.0; 1H NMR (CDCl3, 500 MHz): δ 3.15 (t, 4H), 3.85 (t, 4H), 6.87 (dd, 1H), 6.96-7.00 (m, 1H), 7.20 (d, 1H), 7.22-7.25 (m, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07902239B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-4fcfbfd189614470b9d6d45029dd6011
Quellennotizuspto-grants-2011_03