Ammonium Hydroxide → HCID 12070532, compound

HRID 2182110Notes

Reaction equation

HRID 2182110 reaction equation
[F:1][C:2]1(F)[C:15](F)([F:16])[C:14]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:8]2[C:3]1=[CH:4][CH:5]=[CH:6][CH:7]=2.[NH4+].[OH-]>C1COCC1.[Zn]>[F:1][C:2]1[C:3]2[C:8]([C:9]3[CH:10]=[CH:11][CH:12]=[CH:13][C:14]=3[C:15]=1[F:16])=[CH:7][CH:6]=[CH:5][CH:4]=2

Participants

5

Reactant 2

HCID 14923Ammonium HydroxideHCID 120705359,9,10,10-tetrafluoro-9,10-dihydrophenanthrene

Product 1

HCID 12070532HCID 12070532, compoundYield 95.2%

Reagents, catalysts & solvents 2

HCID 23994ZincCatalystHCID 8028TetrahydrofuranSolvent

Procedure

A solution of the 9,9,10,10-tetrafluoro-9,10-dihydrophenanthrene (1.96 g, 7.75 mmol) in THF (15 ml) was treated with 30% aqueous NH4OH (30 ml) and zinc (2.52 g, 38.75 mmol) and stirred under N2 for 24 hours at room temperature. The reaction was monitored by GC/MS for disappearance of the starting material and found to be complete. The solution was filtered, extracted with hexane (30 ml), and filtered through a short silica column (20 g). The hexane solution was evaporated in vacuo to afford an oil. This crystallized on cooling to room temperature to afford 1.58 g (95% yield) of product.

Workup

  1. filtrationThe solution was filtered
  2. extractionextracted with hexane (30 ml)
  3. filtrationfiltered through a short silica column (20 g)
  4. customThe hexane solution was evaporated in vacuo
  5. customto afford an oil
  6. customThis crystallized
  7. temperatureon cooling to room temperature

Sources & evidence

ORD record
ord-ab58eabb308440fc83fcf4541af6d9c7
Source dataset
uspto-grants-2005_05
Patent number
US06894200B2

Reaction notes

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