Sodium Hydroxide → HCID 15484979, compound

HRID 1251376Notes

Reaction equation

HRID 1251376 reaction equation
C([O:3][C:4](=[O:23])[C:5]([S:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1)([CH3:13])[CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)C.[OH-].[Na+]>CO>[CH3:22][O:21][C:18]1[CH:17]=[CH:16][C:15]([S:14][C:5]([CH3:13])([CH2:6][C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[C:4]([OH:23])=[O:3])=[CH:20][CH:19]=1

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 54165552HCID 54165552, compound

Product 1

HCID 15484979HCID 15484979, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

2-(4-methoxy-phenylsulfanyl)-2-methyl-3-phenyl-propionic acid ethyl ester (4.12 g, 12 mmol) dissolved in methanol (50 ml) and 10 N NaOH (20 ml) was added. The reaction was allowed to stir overnight at room temperature. The reaction mixture was concentrated, diluted with 1:1 hexane:diethyl ether and extracted with H2O. The water layer was cooled with ice and is acidified to pH 3. The acid was then extracted with chloroform and the organic layer was dried over MgSO4, filtered and concentrated to afford of 2-(4-methoxy-phenylsulfanyl)-2-methyl-3-phenyl-propionic acid as a low melting solid. Yield 580 mg, 16%; MS: 303.2 (M+H)+.

Workup

  1. concentrationThe reaction mixture was concentrated
  2. additiondiluted with 1:1 hexane
  3. extractiondiethyl ether and extracted with H2O
  4. temperatureThe water layer was cooled with ice
  5. extractionThe acid was then extracted with chloroform
  6. dry with materialthe organic layer was dried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-b850e08a17c349c0b640116c81ab1f8b
Source dataset
uspto-grants-2002_01
Patent number
US06342508B1

Reaction notes

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