HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654552Generated: October 30, 2026
4-Hydroxybenzaldehyde → 4-(6-Hydroxyhexoxy)benzaldehyde
https://huagongshe.com/reaction/1654552
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Chloro-1-hexanol | HCID 74828 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(6-Hydroxyhexoxy)benzaldehyde | HCID 15051082 | — |
Reaction Steps
2.44 g (0.02 mol) of 4-hydroxybenzaldehyde, 2.73 g (0.02 mol) of 6-chlorohexanol, 1.66 g (0.012 mol) of potassium carbonate and 20 ml of N,N-dimethylformamide were put in a three-neck 50 ml-flask equipped with a stirrer and a thermometer and heated at 100° C. for 2 hours with stirring. The reaction mixture was cooled to room temperature, poured into water containing ice and extracted with ethyl acetate. The resulting extract was dried with anhydrous sodium sulfate, and ethyl acetate was removed therefrom by distillation. The oily residue was allowed to stand at room temperature, whereupon it gradually crystallized. By silica gel thin layer chromatography (using a developer of ethyl acetate), the purity of the crystals was high. The yield of the product was 4.4 g (99.0%).
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-bae6eb3f9ee34a86b3740ed70cb32abd |
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| Source note | uspto-grants-1995_04 |
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