HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058090Generated: November 1, 2026
Dimethylformamide → 4-{2-[Methyl(pyridin-2-yl)amino]ethoxy}benzaldehyde
https://huagongshe.com/reaction/1058090
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | 2-(N-Methyl-N-(2-pyridyl)amino)ethanol | HCID 737420 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-{2-[Methyl(pyridin-2-yl)amino]ethoxy}benzaldehyde | HCID 10422546 | 88% |
Reaction Steps
In a 2l three necked, round bottom flask, 500 ml dimethylformamide is added, followed by addition of 100 g of 2-(N-methyl-N-(2-pyridyl)amino)ethanol (II) and 100 g of 4-fluorobenzaldehyde (III) was added to the reaction mixture and it was stirred for 10 minutes at room temperature and 80 g of potassium tertiary butoxide was added to the reaction mixture. The reaction was monitored by TLC. After completion of the reaction, the reaction mixture was cooled to 5-10° C. and under the cold conditions, 1.5 l of water was added and stirred for 15 min. The mixture was extracted with 4×500 ml of ethyl acetate. The combined organic layer was washed with 3×1 l water. The organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure to give 148 g (88%) of 4-[2-(N-methyl-N-(2-pyridyl)amino)ethoxy)benzaldehyde (IV).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06515132B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-b8953ad80de546a5b001355f2dbfc465 |
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| Source note | uspto-grants-2003_02 |
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