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Bromine → 6-(Trifluoromethyl)pyridazin-3(2H)-one

HRID 877222
Notes
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Reaction equation

HRID 877222 reaction equation
[F:1][C:2]([F:11])([F:10])[C:3]1[CH2:4][CH2:5][C:6](=[O:9])[NH:7][N:8]=1.BrBr>C(O)(=O)C>[F:11][C:2]([F:1])([F:10])[C:3]1[CH:4]=[CH:5][C:6](=[O:9])[NH:7][N:8]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24408BromineHCID 497606526-(Trifluoromethyl)-4,5-dihydropyridazin-3(2H)-one

Product 1

HCID 336982986-(Trifluoromethyl)pyridazin-3(2H)-one

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Conditions

Temperature
100 °C

Procedure

2.6 g (15.65 mmol) of 6-(trifluoromethyl)-4,5-dihydropyridazin-3(2H)-one were dissolved in 20 ml of glacial acetic acid, and the mixture was heated to 100° C. 0.81 ml (15.65 mmol) of bromine was then slowly added dropwise to the solution, and the mixture was stirred at 100° C. for 4 hours. After cooling of the reaction solution, the solvent was removed under reduced pressure and the residue obtained was purified chromatographically on silica gel (mobile phase dichloromethane/methanol 50:1→20:1). This gave 1.34 g (8.15 mmol, 52% of theory) of the title compound.

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Workup

  1. temperatureAfter cooling of the reaction solution
  2. customthe solvent was removed under reduced pressure
  3. customthe residue obtained
  4. customwas purified chromatographically on silica gel (mobile phase dichloromethane/methanol 50:1→20:1)

Sources & evidence

ORD record
ord-2b40619c3fd7440fb762b3e827ee9f1b
Source dataset
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08987256B2

Reaction notes

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