Sodium Hydroxide → 5-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carboxylic acid

HRID 1360547Notes

Reaction equation

HRID 1360547 reaction equation
[OH-].[Na+].[C:3]1([S:9]([CH2:12][CH2:13][CH2:14][C:15]2[N:19]([CH2:20][CH2:21][CH2:22][CH3:23])[N:18]=[C:17]([C:24]([O:26]CC)=[O:25])[CH:16]=2)(=[O:11])=[O:10])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>C(O)C>[C:3]1([S:9]([CH2:12][CH2:13][CH2:14][C:15]2[N:19]([CH2:20][CH2:21][CH2:22][CH3:23])[N:18]=[C:17]([C:24]([OH:26])=[O:25])[CH:16]=2)(=[O:11])=[O:10])[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 66959126ethyl 5-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carboxylate

Product 1

HCID 669583705-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carboxylic acidYield 85.4%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Sodium hydroxide (12 mL, 6M) was added to a solution of ethyl 5-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carboxylate (13.3 g, 35.1 mmol) in 100 mL of ethanol and heated to reflux overnight. The reaction mixture was concentrated under reduced pressure and the residue was diluted with 100 mL of water. The aqueous layer was extracted with several portions of ethyl acetate. The pH of the aqueous layer was adjusted to approximately 2-3 with aqueous hydrochloric acid and was then extracted with several portions of ethyl acetate. The combined organic layers originating from extraction of the aqueous layer were washed with brine, dried over magnesium sulfate, filtered, and concentrated to afford 10.5 g of 5-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carboxylic acid.

Workup

  1. temperatureheated
  2. temperatureto reflux overnight
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. additionthe residue was diluted with 100 mL of water
  5. extractionThe aqueous layer was extracted with several portions of ethyl acetate
  6. extractionwas then extracted with several portions of ethyl acetate
  7. extractionThe combined organic layers originating from extraction of the aqueous layer
  8. washwere washed with brine
  9. dry with materialdried over magnesium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated

Sources & evidence

ORD record
ord-41ce24a7ca8b4df6a0735e5dc7c83100
Source dataset
uspto-grants-2011_02
Patent number
US07879849B2

Reaction notes

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