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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644125Generated: October 26, 2026

Hydrochloric Acid → 2,3,3-Trifluoro-1-Hydroxy-4-n-Propylbicyclo[2.2.2]octane

https://huagongshe.com/reaction/1644125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant2,3,3-Trifluoro-1-Pentylcarbonyloxy-4-n-Propylbicyclo[2.2.2]octaneHCID 59480847—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product2,3,3-Trifluoro-1-Hydroxy-4-n-Propylbicyclo[2.2.2]octaneHCID 59480882—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2,3,3-trifluoro-1-pentylcarbonyloxy-4-n-propylbicyclo[2.2.2]octane (3) (0.12 g), potassium hydroxide (0.11 g), water (0.5 mL) and ethanol (2.0 mL) was stirred at 70° C. for 20 minutes. The mixture was neutralized with hydrochloric acid, added with ethyl acetate (30 mL), and the organic layer was washed with aqueous sodium hydrogen carbonate solution. The organic layer was dried over anhydrous magnesium sulfate, the solvent was vaporized off under reduced pressure, to thereby obtain a crude product. The crude produce was purified by silica gel column chromatography (hexane/ethyl acetate=3:1), to thereby obtain 2,3,3-trifluoro-1-hydroxy-4-n-propylbicyclo[2.2.2]octane (4) (yield=82 mg, yield ratio=98%) as a colorless clear solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124196B2
Source datasetuspto-grants-2012_02
ORD IDord-095bf197376a4411aa409d26019d4840
Source noteuspto-grants-2012_02