Methanol → Methyl 2-(3-mercaptophenyl)acetate

HRID 1785206ノート

反応式

HRID 1785206 の反応式
[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+].CO>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

参加物

5

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-eaefda6315aa49f8be75e652650e3d79
出典データセット
uspto-grants-2009_03
特許番号
US07504433B2

反応ノート

読み込み中…