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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1498664Generated: November 2, 2026

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

https://huagongshe.com/reaction/1498664

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 numberUS09199990B2
Source datasetuspto-grants-2015_12
ORD IDord-8f06701c7c9347519155a261d48f88e8
Source noteuspto-grants-2015_12