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Hydrochloric Acid → HCID 18985350, compound

HRID 1461021
Notes
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Reaction equation

HRID 1461021 reaction equation
[OH-].[Na+].[F:3][C:4]1[C:14]([O:15][C:16]([F:19])([F:18])[F:17])=[C:13]([F:20])[C:12]([F:21])=[CH:11][C:5]=1[C:6]([O:8]CC)=[O:7].Cl>C(O)C>[F:3][C:4]1[C:14]([O:15][C:16]([F:17])([F:18])[F:19])=[C:13]([F:20])[C:12]([F:21])=[CH:11][C:5]=1[C:6]([OH:8])=[O:7]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 18985348HCID 18985348, compound

Product 1

HCID 18985350HCID 18985350, compoundYield 87.4%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

19.3 ml (0.0193 moles) of a 1N aqueous solution of sodium hydroxide were added to a solution of 5.05 g (0.0175 moles) of ethyl 2,4,5-trifluoro-3-trifluoromethoxybenzoate [(XXVIII), X=X'=F, R16 =C2H5O] [prepared as described in step (b) above] in 100 ml of ethanol, and the mixture was allowed to stand at room temperature for 2 hours. At the end of this time, 19.3 ml of 1N aqueous hydrochloric acid were added, and then the reaction mixture was concentrated by evaporation under reduced pressure. The residue was then extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate, and evaporated to dryness under reduced pressure, to give 3.98 g of 2,4,5-trifluoro-3-trifluoromethoxybenzoic acid as a colorless powder.

Workup

  1. concentrationthe reaction mixture was concentrated by evaporation under reduced pressure
  2. extractionThe residue was then extracted with ethyl acetate
  3. washThe extract was washed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. customevaporated to dryness under reduced pressure

Sources & evidence

ORD record
ord-16742694fe654275a87b0c6093b1daa6
Source dataset
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05073556

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes