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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,3,3-Trifluoro-1-Pentylcarbonyloxy-4-n-Propylbicyclo[2.2.2]octane | HCID 59480847 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,3,3-Trifluoro-1-Hydroxy-4-n-Propylbicyclo[2.2.2]octane | HCID 59480882 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124196B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-095bf197376a4411aa409d26019d4840 |
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| Source note | uspto-grants-2012_02 |
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