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Water → 2-Benzyl-3-(tert-butylsulfonyl)propanoic acid

HRID 1034448
Notes
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Reaction equation

HRID 1034448 reaction equation
[CH2:1]([CH:8]([CH2:12]C(C)(C)C)[C:9]([OH:11])=S)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[S:17]([O-:22])(O[O-])(=O)=[O:18].[K+].[K+].[OH2:25]>CO>[CH2:1]([CH:8]([CH2:12][S:17]([C:2]([CH3:7])([CH3:3])[CH3:1])(=[O:22])=[O:18])[C:9]([OH:11])=[O:25])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962Water2×HCID 10313463Potassium peroxymonosulphateHCID 178418656HCID 178418656, compound

Product 1

HCID 141580582-Benzyl-3-(tert-butylsulfonyl)propanoic acidYield 82%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

280 mg of 2-benzyl-3-tert.-butylthio-propionic acid was dissolved in 5 ml of methanol and, while cooling with ice, 1 g of potassium peroxomonosulfate in 4 ml of water was added and the whole was stirred overnight at room temperature. The solution was diluted with water and extracted with methylene chloride, and the extracts were dried and concentrated by evaporation (260 mg, 82% yield).

Workup

  1. additionwas added
  2. extractionextracted with methylene chloride
  3. customthe extracts were dried
  4. concentrationconcentrated by evaporation (260 mg, 82% yield)

Sources & evidence

ORD record
ord-c3793910c873424581c865efc9faa699
Source dataset
uspto-grants-1994_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05317039

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes