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Ethyl Acetate → HCID 178510661, compound

HRID 1591086
Notes
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Reaction equation

HRID 1591086 reaction equation
[C:1]([C:3]1[NH:7][C:6]([C:8]2[C:13]([Cl:14])=[CH:12][C:11]([C:15]([F:18])([F:17])[F:16])=[CH:10][C:9]=2[Cl:19])=[N:5][CH:4]=1)#[N:2].[Br:20]Br.C(OCC)(=O)C>ClC(Cl)C(Cl)Cl>[Br:20][C:4]1[N:5]=[C:6]([C:8]2[C:13]([Cl:14])=[CH:12][C:11]([C:15]([F:17])([F:16])[F:18])=[CH:10][C:9]=2[Cl:19])[NH:7][C:3]=1[C:1]#[N:2]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 8857Ethyl AcetateHCID 24408BromineHCID 189476905-Cyano-2-(2,6-dichloro-4-trifluoromethylphenyl)imidazole

Product 1

HCID 178510661HCID 178510661, compoundYield 169.2%

Reagents, catalysts & solvents 1

HCID 65911,1,2,2-TetrachloroethaneSolvent

Conditions

Temperature
90 °C

Procedure

A mixture of 5-cyano-2-(2,6-dichloro-4-trifluoromethylphenyl)imidazole (1.0 g, 0.0033 mol) and bromine (1.9 g, 0.64 ml, 0.13 mol) in 1,1,2,2-tetrachloroethane (20 ml) was stirred and heated at 90° C. for 7 hours. Ethyl acetate (50 ml) was added and the solution was washed with water (50 ml), aqueous sodium metabisulphite solution (50 ml), water (50 ml), dried over anhydrous sodium sulphate and evaporated to dryness. The solid residue was purified by chromatography on silica gel eluting with a mixture of ethyl acetate and petroleum ether (b.p. 60°-80° C.)(3:10) to give 4-bromo-5-cyano-2-(2,6-dichloro-4-trifluoromethylphenyl)imidazole (2.15 g) as a white solid m.p. 270.5°-272° C.

Workup

  1. washthe solution was washed with water (50 ml), aqueous sodium metabisulphite solution (50 ml), water (50 ml)
  2. dry with materialdried over anhydrous sodium sulphate
  3. customevaporated to dryness
  4. customThe solid residue was purified by chromatography on silica gel eluting with a mixture of ethyl acetate and petroleum ether (b.p. 60°-80° C.)(3:10)

Sources & evidence

ORD record
ord-db3672d63810403e9d4c71056e07b9b2
Source dataset
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05206257

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes