HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104306Generated: October 30, 2026
Water → 4-[3-(Perfluorooctyl)-1-propyloxy]benzaldehyde
https://huagongshe.com/reaction/2104306
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Perfluorooctyl)propyl iodide | HCID 11157582 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[3-(Perfluorooctyl)-1-propyloxy]benzaldehyde | HCID 12154169 | 91% |
Reaction Steps
A 500 mL 2-neck flask equipped with thermometer and gas inlet charged with potassium carbonate (27.6 g), hydroxy benzaldehyde (13.4 g), and 3-(perfluorooctyl)propyl iodide (58.8 g) in DMF (200 mL) was heated to 65° C. (internal temperature). The mixture was stirred at 65° C. until the reaction was complete. The reaction mixture was cooled to room temperature. Water (300 mL) and ether (300 mL) were added and the mixture stirred vigorously for 5 min. The layers were separated and the organic layer retained. The aqueous layer was extracted with ether (3×200 mL). The combined organic layers were washed with water (2×100 mL), Na2S2O3 (1×100 mL), 2.5 N NaOH (3×100 mL), and aqueous NaCl (1×100 mL). The organic layer was dried over MgSO4, filtered and concentrated. The product was further dried under high vacuum for 5 h to give desired product (53 g, 91% yield). The structure of the product was characterized 1H NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576245B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-defe4046821d4c0aa6626f66ab256746 |
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| Source note | uspto-grants-2009_08 |
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