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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSalicylaldehydeHCID 6998—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Perfluorooctyl)propyl iodideHCID 11157582—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4-[3-(Perfluorooctyl)-1-propyloxy]benzaldehydeHCID 1215416991%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576245B2
Source datasetuspto-grants-2009_08
ORD IDord-defe4046821d4c0aa6626f66ab256746
Source noteuspto-grants-2009_08