HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131271Generated: October 30, 2026
Vanillin → 3-Methoxy-4-(2-morpholin-4-yl-ethoxy)-benzaldehyde
https://huagongshe.com/reaction/131271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) | HCID 77210 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methoxy-4-(2-morpholin-4-yl-ethoxy)-benzaldehyde | HCID 874621 | 85% |
Reaction Steps
To a solution of vanilin (76.1 g) in N,N-dimethylformamide (500 mL) is added successively 4-(2-chloroethyl)morpholine hydrochloride (130 g), sodium iodide (7.5 g), and potassium carbonate (207 g). The mixture is stirred at 80° C. for 15 hours. The reaction mixture is concentrated in vacuo. The residue is diluted with ethyl acetate, washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. To the residue is added diisopropyl ether and the resultant crystals are collected by filtration to give 3-methoxy-4-(2-morpholinoethoxy)-benzaldehyde (112.6 g, yield; 85%) as orange crystals. MS (APCI) m/z: 266 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384952B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-061c5ac602954d358e09e4c3aad3133d |
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| Source note | uspto-grants-2008_06 |
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