HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → Heptafluoro-2-naphthol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Perfluoronaphthalene | HCID 67564 | — |
| Solvent | Water | HCID 962 | — |
| Product | Heptafluoro-2-naphthol | HCID 2724940 | 72% |
Reaction Steps
For about 3.5 hours, a mixture of 25 g octafiuoronaphthalene (PCR Inc.; Gainesville, Fla.), 12 g KOH, and 100 mL tertiary butyl alcohol was refluxed. Water was added, and the tertiary butyl alcohol was distilled from the reaction mixture. The residue remaining in the flask was acidified with HCl and the aqueous mixture was extracted three times with 75 mL dichloromethane. The combined extracts were washed twice with 150 mL distilled water, dried over MgSO4, and rotary evaporated to yield a semi-crystalline solid. Recrystallization from hot bexanes gave 18 g heptafluoro-2-naphthol (72% yield) as slightly tan colored crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313245B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-d5a45ffdd446416eae6565f65c803e93 |
| Source note | uspto-grants-2001_11 |