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Sodium Hydroxide → 2-Methyloxazole-4-carboxylic acid

HRID 882776
Notes
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Reaction equation

HRID 882776 reaction equation
C[O:2][C:3]([C:5]1[N:6]=[C:7]([CH3:10])[O:8][CH:9]=1)=[O:4].[OH-].[Na+]>CCO>[CH3:10][C:7]1[O:8][CH:9]=[C:5]([C:3]([OH:4])=[O:2])[N:6]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 10855551methyl 2-methyloxazole-4-carboxylate

Product 1

HCID 5394042-Methyloxazole-4-carboxylic acid

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A solution of the respective 2-acetylamino-3-oxo-propionic acid methyl ester derivative (0.63 mmol, 1.0 eq.) in CHCl3 (0.4 mL) was cooled to 0° C. in an ice/NaCl bath. SOCl2 (0.88 mmol, 1.4 eq.) was added to the stirred solution and the temperature was maintained at 0° C. for 30 minutes. Then the solution was stirred and refluxed for one hour. Another 0.25 eq. of SOCl2 was added and the reaction mixture was refluxed for another hour. The excess SOCl2 was quenched with 1M aq. K2CO3. The aq. layer was extracted twice with ether. The combined organic phases were washed once with water and dried over MgSO4, filtered and concentrated yielding the corresponding 2-methyl-oxazole-4-carboxylic acid methyl ester derivative. The respective 2-methyl-oxazole-4-carboxylic acid methyl ester derivative was dissolved in a mixture of EtOH (0.7 ml) and 2N aq. NaOH (0.7 mL, 2.5 eq.). The mixture was stirred at rt for 2 hours. The reaction mixture was washed once with ether and this organic layer was discarded. The aq. layer was then acidified with conc. HCl and extracted twice with ether. Both organic layers were combined, dried over MgSO4 and concentrated in vacuo to afford the corresponding 2-methyl-oxazole-4-carboxylic acid derivatives.

Workup

  1. washThe reaction mixture was washed once with ether
  2. extractionextracted twice with ether
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-78c46c900f6d40a3b3a8fabf2365f610
Source dataset
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08236801B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes