HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654551Generated: November 2, 2026
4-Hydroxybenzaldehyde → Benzaldehyde, 4-(2-hydroxyethoxy)-
https://huagongshe.com/reaction/1654551
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzaldehyde, 4-(2-hydroxyethoxy)- | HCID 89178 | — |
Reaction Steps
12.2 g (0.1 mol) of 4-hydroxybenzaldehyde, 16.6 g (0.12 mol) of potassium carbonate and 100 ml of N,N-dimethylformamide were put in a three-neck 300 ml-flask equipped with a thermometer and a stirrer and heated up to 60° C. To this mixture was dropwise added 25.0 g (0.2 mol) of 2-bromoethanol. The internal temperature rose up to 80° C. due to the reaction heat. Afterwards, the reaction system was heated and stirred at 100° C. for 2 hours. The reaction mixture was cooled to room temperature, poured into water and extracted with ethyl acetate. The resulting extract was dried with anhydrous sodium sulfate, and ethyl acetate was removed therefrom by distillation. The residue was subjected to silica gel column chromatography (using an eluent of ethyl acetate/n-hexane of 1/1) to obtain the intended 4-(2-hydroxyethoxy)benzaldehyde as an oily product. The yield of the product was 5.8 g (34.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05408009 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-4a3ac83609654d238f7a5a975d752e54 |
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| Source note | uspto-grants-1995_04 |
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