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Sodium hydride → 1-(4'-Ethoxy-2',3'-Difluorophenyl)Methyloxy-2,2,3,3-Tetrafluoro-4-n-Propylbicyclo[2.2.2]octane

HRID 1644130
Notes
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Reaction equation

HRID 1644130 reaction equation
[F:1][C:2]1([F:16])[C:7]([F:9])([F:8])[C:6]2([CH2:12][CH2:13][CH3:14])[CH2:10][CH2:11][C:3]1([OH:15])[CH2:4][CH2:5]2.Br[CH2:18][C:19]1[CH:24]=[CH:23][C:22]([O:25][CH2:26][CH3:27])=[C:21]([F:28])[C:20]=1[F:29].[H-].[Na+].[Cl-].[NH4+]>CN(C)C=O>[CH2:26]([O:25][C:22]1[CH:23]=[CH:24][C:19]([CH2:18][O:15][C:3]23[CH2:4][CH2:5][C:6]([CH2:12][CH2:13][CH3:14])([CH2:10][CH2:11]2)[C:7]([F:9])([F:8])[C:2]3([F:16])[F:1])=[C:20]([F:29])[C:21]=1[F:28])[CH3:27]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 229135944-Ethoxy-2,3-difluorobenzyl bromideHCID 594809982,2,3,3-Tetrafluoro-1-Hydroxy-4-n-Propylbicyclo[2.2.2]octane

Product 1

HCID 594809461-(4'-Ethoxy-2',3'-Difluorophenyl)Methyloxy-2,2,3,3-Tetrafluoro-4-n-Propylbicyclo[2.2.2]octane

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

2,2,3,3-Tetrafluoro-1-hydroxy-4-n-propylbicyclo[2.2.2]octane (12) (0.15 g), and 4-bromomethyl-1-ethoxy-2,3-difluorobenzene (5) (0.31 g) were added to a dimethyl formamide suspension (2.0 mL) of sodium hydride (18 mg), the mixture was stirred at room temperature for 6 hours, and then added with saturated aqueous ammonium chloride solution to thereby terminate the reaction. The organic layer was extracted three times with ethyl acetate, the organic layers were combined, and washed with saturated sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate, and the solvent was vaporized off under reduced pressure to thereby obtain a crude product. The crude product was purified by silica gel column chromatography (hexane/ethyl acetate=9:1), to thereby obtain 1-(4′-ethoxy-2′,3′-difluorophenyl)methyloxy-2,2,3,3-tetrafluoro-4-n-propyl bicyclo[2.2.2]octane (13) (yield=0.15 g, yield ratio=58%) as a colorless clear crystal.

Workup

  1. customto thereby terminate
  2. customthe reaction
  3. extractionThe organic layer was extracted three times with ethyl acetate
  4. washwashed with saturated sodium chloride solution
  5. dry with materialThe organic layer was dried over anhydrous sodium sulfate

Sources & evidence

ORD record
ord-3b4a6ef40b9946229829eaacf385dd71
Source dataset
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08124196B2

Reaction notes

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