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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041652Generated: October 31, 2026

Dichloromethane → 3-(5-Morpholin-4-yl-2-nitro-phenoxy)-propionitrile

https://huagongshe.com/reaction/1041652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CyanideHCID 8929—
Reactant4-[3-(2-Bromo-ethoxy)-4-nitro-phenyl]-morpholineHCID 67263697—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product3-(5-Morpholin-4-yl-2-nitro-phenoxy)-propionitrileHCID 6726348357%

Reaction Steps

Sodium cyanide (79 mg, 1.6 mmol) was added to 4-[3-(2-Bromo-ethoxy)-4-nitro-phenyl]-morpholine (447 mg, 1.35 mmol) in Dimethyl sulfoxide (5 mL) and the reaction was stirred at room temperature 48 h. The mixture was diluted with 50 mL Et2O and 20 mL water. DCM was added to solubilize ppt. The layers were separated and the aq. extracted 3×50 mL DCM. The combined organic extracts were washed with satd. sodium bicarbonate (50 mL) and brine (50 mL), conc. in vacuo and taken up in DCM for application to a 25 g SiO2 pre-load cartridge. Chromatography (0-100% EtOAc:Hex) afforded 3-(5-Morpholin-4-yl-2-nitro-phenoxy)-propionitrile as a yellow solid (212 mg, 57%). 1H-NMR (CDCl3): 8.01 (d, 1H, J=9.2 Hz), 6.52 (d, 1H, J=9.2 Hz), 6.40 (s, 1H), 4.31 (t, 2H, J=7.0 Hz), 3.86 (t, 4H, J=4.6 Hz), 3.35 (t, 4H, J=4.6 Hz), 2.93 (t, 2H, J=7.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552186B2
Source datasetuspto-grants-2013_10
ORD IDord-cae0d73f5cbe4020be6c0718322618dd
Source noteuspto-grants-2013_10