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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410378Generated: November 2, 2026

Morpholine → 4-(3-Iodo-5-nitrophenyl)morpholine

https://huagongshe.com/reaction/410378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant1-Fluoro-3-iodo-5-nitrobenzeneHCID 259086—
SolventDimethyl SulfoxideHCID 679—
Product4-(3-Iodo-5-nitrophenyl)morpholineHCID 5845630680%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of 1-fluoro-3-iodo-5-nitrobenzene (4.0 g, 15 mmol) in DMSO (7.5 mL) was added morpholine (3.26 mL, 37.5 mmol), and the mixture (which instantly became purple) was heated to 130° C. for 30 min in the microwave. Purification was attempted by directly loading the mixture onto a silica gel column (80 g; load neat w/CH2Cl2 rinse; 100:0 to 60:40 hexanes:EtOAc over 35 minutes) but the mixture crashed at the top of the column and not all the mixture could be loaded. Nonetheless, after an initial spike in pressure, purification was possible, and the residual material was purified in a second purification (24 g; load w/CH2Cl2; 100:0 to 60:40 hexanes:EtOAc over 20 minutes). Concentration of the combined fractions from the two purifications provided 4-(3-iodo-5-nitrophenyl)morpholine (4.01 g, 12.0 mmol, 80%) as a bright yellow solid. 1H NMR (400 MHz, CDCl3): δ 7.99 (s, 1H); 7.67 (s, 1H); 7.47 (s, 1H); 3.89 (m, 4H); 3.26 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759366B2
Source datasetuspto-grants-2014_06
ORD IDord-5c3d512774cd48889423c50db6f8cecb
Source noteuspto-grants-2014_06