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Water → 2-(4-Bromophenyl)-3,3,3-trifluoronitropropene

HRID 51165
Notes
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Reaction equation

HRID 51165 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[C:9]([F:12])([F:11])[F:10])=[CH:4][CH:3]=1.[CH3:14][N+:15]([O-:17])=[O:16].O>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:9]([F:12])([F:11])[F:10])=[CH:14][N+:15]([O-:17])=[O:16])=[CH:4][CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962WaterHCID 6375NitromethaneHCID 6038664'-Bromo-2,2,2-trifluoroacetophenone

Product 1

HCID 536841792-(4-Bromophenyl)-3,3,3-trifluoronitropropene

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

A stirred solution of 4′-bromo-2,2,2-trifluoroaceto-phenone (0.392 g, 2.00 mmol) and CH3NO2 (0.488 g, 8.0 mmol) in dry toluene (70 mL) containing N,N-diethylenediamine (30 mmol) is heated at reflux with a Dean and Stark trap until complete removal of H2O. The cooled solution is washed with 5% aqueous HCl, dried over MgSO4, filtered, evaporated in vacuo and the resulting residue when purified by chromatography gives the title compound.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. temperatureis heated
  2. washThe cooled solution is washed with 5% aqueous HCl
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. customevaporated in vacuo
  6. customthe resulting residue when purified by chromatography

Sources & evidence

ORD record
ord-dd350a8954c8448d897d9bc677072556
Source dataset
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06713516B2

Reaction notes

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