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Methyl iodide → 1-Bromo-2,4-difluoro-3-methoxybenzene

HRID 1700000
Notes
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Reaction equation

HRID 1700000 reaction equation
[OH:1][C:2]1[C:3]([F:10])=[C:4]([Br:9])[CH:5]=[CH:6][C:7]=1[F:8].[C:11](=O)([O-])[O-].[K+].[K+].CI>CC(C)=O>[CH3:11][O:1][C:2]1[C:3]([F:10])=[C:4]([Br:9])[CH:5]=[CH:6][C:7]=1[F:8]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 183711103-Bromo-2,6-difluorophenol

Product 1

HCID 183711091-Bromo-2,4-difluoro-3-methoxybenzene

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Conditions

Temperature
20 °C

Procedure

A quantity of 3.7 g of 3-hydroxy-2,4-difluoro-bromobenzene is dissolved in 25 ml of acetone and 2.5 g of potassium carbonate is added followed by 2.2 ml of methyl iodide. The mixture is stirred at 20° C. for 6 hours and the solvent evaporated. After addition of dichloromethane, the suspension is filtered. Evaporation of the solvent affords the desired product.

Workup

  1. customthe solvent evaporated
  2. additionAfter addition of dichloromethane
  3. filtrationthe suspension is filtered
  4. customEvaporation of the solvent

Sources & evidence

ORD record
ord-24f5c5162f5c49bf8082deba94f9f7e7
Source dataset
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06348624B1

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes