HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703525Generated: October 31, 2026
4-Hydroxybenzaldehyde → p-(2-(Dimethylamino)ethoxy)benzaldehyde
https://huagongshe.com/reaction/703525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | 2-Chloro-N,N-dimethylethylamine | HCID 7901 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | p-(2-(Dimethylamino)ethoxy)benzaldehyde | HCID 84823 | 71.5% |
Reaction Steps
To a solution of 61.1 g of p-hydroxybenzaldehyde in 240 ml of N,N-dimethylformamide was added 138 g of potassium carbonate, 80.7 g of 2-dimethylaminoethyl chloride and 30 ml of isopropyl ether. The mixture was stirred at 60° C. for 1.5 hours. After cooling, the reaction mixture was poured into 720 ml of water, and the whole was extracted with chloroform. The chloroform layer was extracted with aqueous hydrochloric acid. The aqueous layer was made alkaline with aqueous sodium hydroxide solution and extracted with ethyl acetate. The extract was washed with water, dried and evaporated. The residue was distilled to give 69.1 g of colorless oil, b.p. 142°-144° C. (4 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983633 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-aba9b1ab47284d8baf0d2e74d53d3fa9 |
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| Source note | uspto-grants-1991_01 |
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