Potassium Hydroxide → Methyl 2-(3-mercaptophenyl)acetate

HRID 854538

Reaction equation

HRID 854538 reaction equation
[CH3:1][O:2][C:3](=[O:17])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([S:11]C(=O)N(C)C)[CH:6]=1.[OH-].[K+]>O>[CH3:1][O:2][C:3](=[O:17])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([SH:11])[CH:6]=1

Participants

4

Procedure

A mixture of (3-dimethylcarbamoylsulfanyl-phenyl)-acetic acid methyl ester (2.0 g, 7.9 mmol), potassium hydroxide (1.4 g, 24 mmol) methanol (50 mL), and water (5 mL) is stirred at reflux 3 hr. The mixture is concentrated, and product partitioned between 1M aqueous hydrochloric acid (50 mL) and ethyl acetate (3×75 mL). The combined extracts are dried over anhydrous magnesium sulfate, filtered and concentrated. The residue is taken up in methanol (50 mL), 2 mL concentrated sulfuric acid is added, and the mixture refluxed 3 hr. The mixture is concentrated, and the residue purified by silica chromatography eluting with 7:3 hexanes:ethyl acetate to afford the title compound as a pale yellow oil, 1.0 g, 69%. MS M++1 183. The structure is confirmed by 1H NMR spectroscopy.

Workup

  1. temperatureat reflux 3 hr
  2. concentrationThe mixture is concentrated
  3. customproduct partitioned between 1M aqueous hydrochloric acid (50 mL) and ethyl acetate (3×75 mL)
  4. dry with materialThe combined extracts are dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. addition2 mL concentrated sulfuric acid is added
  8. temperaturethe mixture refluxed 3 hr
  9. concentrationThe mixture is concentrated
  10. customthe residue purified by silica chromatography
  11. washeluting with 7:3 hexanes

Sources & evidence

ORD record
ord-dcf719d375cc495a89cd7ca44e240e01
Source dataset
uspto-grants-2007_08
Patent number
US07259175B2

Linked notes

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