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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555478Generated: October 30, 2026

2-Morpholinoethanol → 3,5-Dimethyl-4-(2-morpholin-4-yl-ethoxy)benzaldehyde

https://huagongshe.com/reaction/555478

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MorpholinoethanolHCID 61163—
Reactant3,5-Dimethyl-4-hydroxybenzaldehydeHCID 75222—
ReactantDiisopropylethylamineHCID 81531—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3,5-Dimethyl-4-(2-morpholin-4-yl-ethoxy)benzaldehydeHCID 2893258032%

Reaction Steps

To a solution of 4-hydroxy-3,5-dimethyl benzaldehyde (3.0 g, 20 mmol) in anhydrous THF (100 mL), triphenyl phosphene (10.49 g, 40 mmol), 4-(2-hydroxyethyl)morpholine (5.25 g, 40 mmol) and N,N-diisopropylethylamine (7.76 g, 60 mmol) were added. To this stirred solution was added diethylazodicarboxylate (6.97 g, 40 mmol). The reaction mixture was stirred at room temperature overnight under nitrogen and diluted with ethyl acetate (200 mL). The organic layer was washed with water and brine and dried over anhydrous Na2SO4. The solvent was removed under reduced pressure. The crude material was purified by column chromatography (silica gel 230-400 mesh; 0-3% methanol in CH2Cl2 as eluent) to give 3,5-dimethyl-4-(2-morpholin-4-yl-ethoxy)benzaldehyde (1.66 g, 32%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053440B2
Source datasetuspto-grants-2011_11
ORD IDord-b70af618ee814bcab03f3456883e15fe
Source noteuspto-grants-2011_11