Sodium Hydroxide → 7-(4-Chlorophenylsulphonamido)-2,2-dimethylheptanoic Acid
Reaction equation
C([O:3][C:4](=[O:24])[C:5]([CH3:23])([CH3:22])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][NH:11][S:12]([C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][CH:16]=1)(=[O:14])=[O:13])C.[OH-].[Na+]>>[Cl:21][C:18]1[CH:17]=[CH:16][C:15]([S:12]([NH:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][C:5]([CH3:23])([CH3:22])[C:4]([OH:24])=[O:3])(=[O:13])=[O:14])=[CH:20][CH:19]=1Participants
3
Procedure
Ethyl-7-(4-chlorophenylsulphonamido)-2,2-dimethylheptanoate (3.5 g, 0.09 mol) was treated with sodium hydroxide by the method described in Example 5(iii) to give the title compound (1.9 g) m.p. 132°-3° C. (dichloroethane/40°-60° petroleum ether).
Sources & evidence
- ORD record
- ord-dff64e4fa3e942e6947bcf2bdd5f997f
- Source dataset
- uspto-grants-1991_03
- Patent number
- US04997847
Reaction notes
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