HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332652Generated: October 26, 2026
3-Hydroxybenzaldehyde → 3-(8-(1,3-Dioxolan-2-yl)octyloxy)benzaldehyde
https://huagongshe.com/reaction/332652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(8-Bromooctyl)-1,3-dioxolane | HCID 11832318 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(8-(1,3-Dioxolan-2-yl)octyloxy)benzaldehyde | HCID 86676897 | 80.7% |
Reaction Steps
To a stirred solution of 2-(8-bromooctyl)-1,3-dioxolane (5 g, 18.85 mmol) in dimethyl formamide (100 mL) was added 3-hydroxybenzaldehyde (2.37 g, 19.42 mmol) and potassium carbonate (5.37 g, 38.83 mmol). The reaction mixture was stirred at 80° C. for 16 hours. The reaction mixture was diluted with water and extracted with ethyl acetate (×3). The combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate solution and brine, dried (sodium sulfate), filtered, and concentrated under reduced pressure. The crude material was purified by silica gel column chromatography eluting with 0-100% ethyl acetate in iso-hexane to afford the title compound (4.66 g, 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877774B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-7ea8671f9a0a407fa9595951e2b5b456 |
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| Source note | uspto-grants-2014_11 |
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