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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Reactant | 3,5-Dimethyl-4-hydroxybenzaldehyde | HCID 75222 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3,5-Dimethyl-4-(2-morpholin-4-yl-ethoxy)benzaldehyde | HCID 28932580 | 32% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053440B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-b70af618ee814bcab03f3456883e15fe |
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| Source note | uspto-grants-2011_11 |
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