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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896728Generated: October 25, 2026

Water → 4-Heptadecafluorooctyl-phenol

https://huagongshe.com/reaction/896728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantPerfluorooctyl iodideHCID 10491—
Reactant4-IodophenylacetateHCID 141793—
CatalystIodineHCID 807—
CatalystCopperHCID 23978—
SolventDimethyl SulfoxideHCID 679—
Product4-Heptadecafluorooctyl-phenolHCID 1098406666.7%

Reaction Conditions

Temperature105 °C

Reaction Steps

To a solution of acetic acid 4-iodo-phenyl ester (9 gm, 0.0366 mol) in anhydrous DMSO (75 mL) was added copper powder (5.8 g, 0.091 mol), perfluorooctyl iodide (25 g, 0.046 mol) and iodine (130 mg). The reaction mixture was heated to 105° C. for 18 hr, cooled, combined with 100 ml water and 50 ml ether and filtered to remove insoluble copper salts. The organic and aqueous layers in the filtrate were separated, and the aqueous layer extracted twice with ether (2×100 mL). The combined organics were washed with water and brine, dried over MgSO4, and concentrated. To a solution of the crude product in 50 mL methanol was added 1.5 mL 10N HCl. The mixture was refluxed on a steam bath for 1 hr to hydrolyze the acetate completely to the phenol. After cooling to room temperature, the reaction mixture was poured into a separatory funnel containing 100 mL water, and extracted with ether (3×75 mL). The combined organics were washed with water and brine and dried over MgSO4. Recrystallization of the crude concentrate gave 12.5 g of the phenol at 99% purity by HPLC as a waxy solid mp 63-68° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919404B2
Source datasetuspto-grants-2005_07
ORD IDord-fa91d1a84e2a416cb83219751f07c7a2
Source noteuspto-grants-2005_07