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2-Fluoropyridine → 2-{1-Methyl-2-[4-(3,5-difluorophenoxy)phenoxy]ethoxy}pyridine

HRID 1073514
Notes
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Reaction equation

HRID 1073514 reaction equation
[H-].[Na+].[CH3:3][CH:4]([OH:22])[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][C:14]2[CH:19]=[C:18]([F:20])[CH:17]=[C:16]([F:21])[CH:15]=2)=[CH:9][CH:8]=1.[H][H].F[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=1>CN(C)C=O.O>[CH3:3][CH:4]([O:22][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=1)[CH2:5][O:6][C:7]1[CH:8]=[CH:9][C:10]([O:13][C:14]2[CH:15]=[C:16]([F:21])[CH:17]=[C:18]([F:20])[CH:19]=2)=[CH:11][CH:12]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 97462-FluoropyridineHCID 24758Sodium hydrideHCID 134559131-Methyl-2-[4-(3,5-difluorophenoxy)phenoxy]ethanolHCID 178418361HCID 178418361, compound

Product 1

HCID 133867412-{1-Methyl-2-[4-(3,5-difluorophenoxy)phenoxy]ethoxy}pyridineYield 72.2%

Reagents, catalysts & solvents 2

HCID 962
Water
Solvent
HCID 6228DimethylformamideSolvent2×

Procedure

To a suspension of sodium hydride (20 mg, 0.5 mmol; 60% in oil) in dimethylformamide (1 ml), a solution of 1-methyl-2-[4-(3,5-difluorophenoxy)phenoxy]ethanol (140 mg, 0.5 mmol) in dimethylformamide (1 ml) was dropwise added with stirring, and stirring was continued at room temperature until the generation of hydrogen gas ceased. 2-Fluoropyridine (97 mg, 1.0 mmol) was dropwise added thereto, and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water (40 ml) and extracted with toluene (20 ml) three times. The toluene layer was dried over anhydrous magnesium sulfate, and the solvent was removed by evaporation. The residue was purified by silica gel column chromatography to give 2-{1-methyl-2-[4-(3,5-difluorophenoxy)phenoxy]ethoxy}pyridine (129 mg) as pale yellow liquid. nD19.0 1.5602.

Workup

  1. stirringstirring
  2. stirringthe mixture was stirred at room temperature overnight
  3. extractionextracted with toluene (20 ml) three times
  4. dry with materialThe toluene layer was dried over anhydrous magnesium sulfate
  5. customthe solvent was removed by evaporation
  6. customThe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-f2be74fed7cf411bb7996e7cf4c9f291
Source dataset
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04970222

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes