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Sodium Hydroxide → 3-Ethoxy-4-(1-methylpyrazol-4-yl)benzoic acid

HRID 1096996
Notes
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Reaction equation

HRID 1096996 reaction equation
[OH-].[Na+].[CH2:3]([O:5][C:6]1[CH:7]=[C:8]([CH:13]=[CH:14][C:15]=1[C:16]1[CH:17]=[N:18][N:19]([CH3:21])[CH:20]=1)[C:9]([O:11]C)=[O:10])[CH3:4].O.Cl>CCOC(C)=O.CCCCCC>[CH2:3]([O:5][C:6]1[CH:7]=[C:8]([CH:13]=[CH:14][C:15]=1[C:16]1[CH:17]=[N:18][N:19]([CH3:21])[CH:20]=1)[C:9]([OH:11])=[O:10])[CH3:4]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 14798Sodium HydroxideHCID 21885828Hydrate;hydrochlorideHCID 57930994Methyl 3-ethoxy-4-(1-methylpyrazol-4-yl)benzoate

Product 1

HCID 579309863-Ethoxy-4-(1-methylpyrazol-4-yl)benzoic acid

Reagents, catalysts & solvents 1

HCID 21226206Ethyl acetate hexaneSolvent

Procedure

Aqueous 5 N sodium hydroxide solution (0.6 mL, 3.0 mmol) was added to a methano chloroform (1/1) solution (5 mL) of methyl 3-ethoxy-4-(1-methylpyrazol-4-yl)benzoate (149 mg, 0.57 mmol), and stirred overnight at room temperature. 5 N hydrochloric acid water (0.6 mL, 3.0 mmol) was added to the reaction liquid. The aqueous layer was extracted twice with chloroform, washed with saturated saline water, and dried with magnesium sulfate. The solution was filtered and concentrated under reduced pressure to obtain the title compound as a white solid.

Workup

  1. extractionThe aqueous layer was extracted twice with chloroform
  2. washwashed with saturated saline water
  3. dry with materialdried with magnesium sulfate
  4. filtrationThe solution was filtered
  5. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-1c68adf64af54482b21060c22f8c2713
Source dataset
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08138197B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes