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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 185Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/185

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 5981783816.14%

Reaction Conditions

Temperature110 °C

Reaction Steps

diacetoxypalladium (0.136 g, 0.60 mmol) was added to a stirred mixture of 1-iodo-3-(2-methoxyethoxy)-5-nitrobenzene (3.9 g, 12.07 mmol), morpholine (1.373 mL, 15.69 mmol) and 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.225 g, 0.36 mmol) and cesium carbonate (11.80 g, 36.21 mmol) dissolved in toluene (100 mL) over a period of 5 minutes, degased and under argon. The resulting mixture was heated at 110 °C for 4 hours.The toluene was evaporated , water ( 50ml) was added and the mixture was extracted with ethyle acetate, dried over MgSO4, filtered and asorbed on silica gel.The crude product was purified by flash chromatography on silica gel eluting with 1 to 4% methanol in dichloromethane. The solvent was evaporated to dryness to afford 4-(3-(2-methoxyethoxy)-5-nitrophenyl)morpholine (0.550 g, 16.14 %) as a orange solid. ( starting material unreacted : 2 .5g)

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-5a683960052443b49da1956ac277ce2a
Source note750 AstraZeneca ELN dataset