p-Toluenesulfonic acid → HCID 10200089, compound

HRID 413899Notes

Reaction equation

HRID 413899 reaction equation
[CH:1]1[CH:6]=[C:5]([S:7]([OH:10])(=[O:9])=[O:8])[CH:4]=[C:3]([NH2:11])[CH:2]=1.[CH2:12]([O:14][C:15](=[O:29])[CH:16]([CH2:20][C:21](=O)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C:17](=O)[CH3:18])[CH3:13].[OH-].[Na+].CC1C=CC(S(O)(=O)=O)=CC=1>C(O)C>[CH2:12]([O:14][C:15]([C:16]1[CH:20]=[C:21]([C:22]2[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=2)[N:11]([C:3]2[CH:2]=[CH:1][CH:6]=[C:5]([S:7]([OH:10])(=[O:8])=[O:9])[CH:4]=2)[C:17]=1[CH3:18])=[O:29])[CH3:13]

Participants

6

Procedure

Metanilic acid (5 mmol, 0.9 g), 3-oxo-2-(2-oxo-2-phenyl-ethyl)-butyric acid ethyl ester (5 mmol, 1.2 g), sodium hydroxide (5 mmol, 0.2 g), and tosic acid (0.1 g) were combined in ethanol, then heated under reflux. The unreacted metanilic acid was precipitated on ice and filtered from the reaction mixture. The filtrate was evaporated to yield an oil, which was purified over silica gel. After standing, the named product solidified as purple crystals (m.p. 94° C.-96° C.).

Workup

  1. temperatureheated
  2. temperatureunder reflux
  3. customThe unreacted metanilic acid was precipitated on ice
  4. filtrationfiltered from the reaction mixture
  5. customThe filtrate was evaporated
  6. customto yield an oil, which
  7. customwas purified over silica gel

Sources & evidence

ORD record
ord-1ab4a4357fa249d4a18d3844f3962796
Source dataset
uspto-grants-2003_05
Patent number
US06569890B2

Reaction notes

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