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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028088Generated: November 1, 2026

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

https://huagongshe.com/reaction/1028088

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 CombiFlash 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 inital 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 (s, 4H); 3.26 (s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735417B2
Source datasetuspto-grants-2014_05
ORD IDord-88b54eb143764aec8ea1d320f3de7c9a
Source noteuspto-grants-2014_05