Hydrochloric Acid → HCID 19759057, compound

HRID 2051215Notes

Reaction equation

HRID 2051215 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-8fc23f0401b449f4bda85bc764d0e24d
Source dataset
uspto-grants-1991_05
Patent number
US05017579

Reaction notes

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