Hydrochloric Acid → HCID 19759057, compound

HRID 1885922Notes

Reaction equation

HRID 1885922 reaction equation
[CH:1]([C:4]1[O:8][N:7]=[C:6]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:5]=1[S:15]([C:18]1[CH:23]=[CH:22][C:21]([O:24]S(C2C=CC(C)=CC=2)(=O)=O)=[CH:20][CH:19]=1)(=[O:17])=[O:16])([CH3:3])[CH3:2].[OH-].[Na+].Cl>C(O)(C)C.O>[OH:24][C:21]1[CH:22]=[CH:23][C:18]([S:15]([C:5]2[C:6]([C:9]3[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=3)=[N:7][O:8][C:4]=2[CH:1]([CH3:3])[CH3:2])(=[O:17])=[O:16])=[CH:19][CH:20]=1

Participants

6

Procedure

A mixture of 2.5 g (0.005 mol) of 5-isopropyl-3-phenyl-4-(4-tosyloxy-benzenesulphonyl)-isoxazole and 0.8 g (0.02 mol) of sodium hydroxide in 20 ml of isopropanol and 10 ml of water was heated under reflux for 2.5 hours. After reacting, the mixture was allowed to cool, diluted with 50 ml of water and acidified with concentrated hydrochloric acid. The product so obtained was suction-filtered and washed with water to obtain 1.4 g of the desired compound which was purified by elution chromatography on silica using chloroform as eluent.

Workup

  1. temperaturewas heated
  2. temperatureunder reflux for 2.5 hours
  3. temperatureto cool
  4. customThe product so obtained
  5. filtrationwas suction-filtered
  6. washwashed with water

Sources & evidence

ORD record
ord-d934167f5e8647ec9c6f4211da40ac13
Source dataset
uspto-grants-1992_09
Patent number
US05147878

Reaction notes

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