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Sodium Hydroxide → 1-(2-fluoroethyl)-1H-pyrazole-5-carboxylic acid

HRID 244670
Notes
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Reaction equation

HRID 244670 reaction equation
[F:1][CH2:2][CH2:3][N:4]1[C:8]([C:9]([O:11]CC)=[O:10])=[CH:7][CH:6]=[N:5]1.[OH-].[Na+]>CO>[F:1][CH2:2][CH2:3][N:4]1[C:8]([C:9]([OH:11])=[O:10])=[CH:7][CH:6]=[N:5]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 58356443Ethyl 1-(2-fluoroethyl)-1H-pyrazole-5-carboxylate

Product 1

HCID 583563241-(2-fluoroethyl)-1H-pyrazole-5-carboxylic acidYield 77.7%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
20 °C

Procedure

To a solution of ethyl 1-(2-fluoroethyl)-1H-pyrazole-5-carboxylate (0.2 g) in methanol (5 ml) was added 2M sodium hydroxide (5 ml) and the mixture stirred at 20° C. for 18 h. The solvent was removed in vacuo and the residue dissolved in water (20 ml) and acidified to pH-4 using 2M hydrochloric acid then extracted with ethyl acetate (20 ml), dried over sodium sulphate and evaporated to give the title compound (0.132 g) as a white solid.

Workup

  1. customThe solvent was removed in vacuo
  2. dissolutionthe residue dissolved in water (20 ml)
  3. extractionthen extracted with ethyl acetate (20 ml)
  4. dry with materialdried over sodium sulphate
  5. customevaporated

Sources & evidence

ORD record
ord-2a1e26f0048a46dd83791a805da69d54
Source dataset
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08658635B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes