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Potassium tert-butoxide → 1-Bromo-4-(1-fluorovinyl)benzene

HRID 1476077
Notes
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Reaction equation

HRID 1476077 reaction equation
CC(C)([O-])C.[K+].[Br:7][C:8]1[CH:13]=[CH:12][C:11]([CH:14]([F:17])[CH2:15]Br)=[CH:10][CH:9]=1>CCCCC>[Br:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]([F:17])=[CH2:15])=[CH:10][CH:9]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 23665647Potassium tert-butoxideHCID 58288379HCID 58288379, compound

Product 1

HCID 582882361-Bromo-4-(1-fluorovinyl)benzene

Reagents, catalysts & solvents 1

HCID 8003PentaneSolvent

Conditions

Temperature
0 °C

Procedure

796 mg (7.09 mmol) of potassium tert-butoxide were added in several portions to a solution, cooled to 0° C., of 1.0 g (3.55 mmol) of 1-bromo-4-(2-bromo-1-fluoroethyl)benzene in 10 ml of pentane. The resulting suspension was stirred at 0° C. for 30 min and then at RT for 1 h. The solid was filtered off, and the filtrate was washed with saturated ammonium chloride solution, dried over magnesium sulphate and carefully concentrated under reduced pressure. This gave 0.61 g (85.6% of theory) of the title compound.

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Workup

  1. waitat RT for 1 h
  2. filtrationThe solid was filtered off
  3. washthe filtrate was washed with saturated ammonium chloride solution
  4. dry with materialdried over magnesium sulphate
  5. concentrationcarefully concentrated under reduced pressure

Sources & evidence

ORD record
ord-2afb83c5d4ca4665a60dfc077f8087f7
Source dataset
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09018414B2

Reaction notes

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