tert-Butanol → Heptafluoro-2-naphthol

HRID 428348Notes

Reaction equation

HRID 428348 reaction equation
[F:1][C:2]1[C:3]([F:18])=[C:4]([F:17])[C:5]([F:16])=[C:6]2[C:11]=1[C:10]([F:12])=[C:9](F)[C:8]([F:14])=[C:7]2[F:15].[OH-].[K+].C([OH:25])(C)(C)C>O>[F:1][C:2]1[C:3]([F:18])=[C:4]([F:17])[C:5]([F:16])=[C:6]2[C:11]=1[C:10]([F:12])=[C:9]([OH:25])[C:8]([F:14])=[C:7]2[F:15]

Participants

5

Reactant 3

HCID 6386tert-ButanolHCID 14797Potassium HydroxideHCID 67564Perfluoronaphthalene

Product 1

HCID 2724940Heptafluoro-2-naphtholYield 72%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

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.

Workup

  1. temperaturewas refluxed
  2. distillationthe tertiary butyl alcohol was distilled from the reaction mixture
  3. extractionthe aqueous mixture was extracted three times with 75 mL dichloromethane
  4. washThe combined extracts were washed twice with 150 mL
  5. distillationdistilled water
  6. dry with materialdried over MgSO4
  7. customrotary evaporated
  8. customto yield a semi-crystalline solid
  9. customRecrystallization from hot bexanes

Sources & evidence

ORD record
ord-d5a45ffdd446416eae6565f65c803e93
Source dataset
uspto-grants-2001_11
Patent number
US06313245B1

Reaction notes

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