Potassium Hydroxide → HCID 178474155, compound
Reaction equation
F[S:2]([CH2:5][CH2:6][NH:7][C:8]1[CH:13]=[C:12]([NH:14][C:15](=[O:17])[CH3:16])[CH:11]=[CH:10][C:9]=1[CH3:18])(=[O:4])=[O:3].[OH-:19].[K+:20]>O>[K:20][CH:5]([S:2]([OH:19])(=[O:4])=[O:3])[CH2:6][NH:7][C:8]1[CH:13]=[C:12]([NH:14][C:15](=[O:17])[CH3:16])[CH:11]=[CH:10][C:9]=1[CH3:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N-(2-Fluorosulfonylethyl-2-methyl-5-acetamidoaniline (13.7 g, 0.05 m) is stirred with water (100 ml.) and potassium hydroxide (5.0 g) at room temperature for 2 hrs. when thin-layer chromatography shows reaction to be complete. The aqueous solution is used in the coupling reaction without further isolation.
Workup
- customreaction
- customThe aqueous solution is used in the coupling reaction without further isolation
Sources & evidence
- ORD record
- ord-5c36bd6f2c1a47e2b51c42c8cfa486c9
- Source dataset
- uspto-grants-1981_08
- Patent number
- US04282144
Reaction notes
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