Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 187Generated: October 23, 2026

Morpholine → 4-[3-(2-Methoxyethoxy)-5-nitrophenyl]morpholine

https://huagongshe.com/en/reaction/187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant1-Iodo-3-(2-methoxyethoxy)-5-nitro-benzeneHCID 59817811—
ReagentCesium carbonateHCID 10796—
CatalystBinap, (A+-)-HCID 634876—
CatalystPalladium (II) acetateHCID 4144353—
SolventTolueneHCID 1140—
Product4-[3-(2-Methoxyethoxy)-5-nitrophenyl]morpholineHCID 5981783853.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

The diacetoxypalladium (0.337 g, 1.50 mmol) was added to a stirred mixture of 1-iodo-3-(2-methoxyethoxy)-5-nitrobenzene (9.7 g, 30.02 mmol), cesium carbonate (29.3 g, 90.07 mmol) and morpholine (3.41 mL, 39.03 mmol) and 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (1.869 g, 3.00 mmol) dissolved in toluene (200 mL) and dioxane (50 mL) The reaction was degased, purged with argon and heated at 110 °C for 15 hours. The mixture was diluted with dichloromethane (250ml) the salts were fitered, the filtrate was concentrated. The crude product was purified by flash chromatography on silica gel eluting with 0 to 15% ethyl acetate in dichloromethane. The solvent was evaporated to dryness to afford 4-(3-(2-methoxyethoxy)-5-nitrophenyl)morpholine (4.50 g, 53.1 %) as a orange solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-ea00f60c7d1b4b2b96c954e87362056a
Source note750 AstraZeneca ELN dataset