Methane → HCID 19108679, compound
Reaction equation
[S:1](Cl)(=[O:4])(=[O:3])[NH2:2].[Cl:6][C:7]1[CH:8]=[C:9]([CH:14]=[CH:15][C:16]=1[Cl:17])[O:10][CH2:11][CH2:12][OH:13].C>C(OC(C)C)(C)C>[Cl:6][C:7]1[CH:8]=[C:9]([CH:14]=[CH:15][C:16]=1[Cl:17])[O:10][CH2:11][CH2:12][O:13][S:1](=[O:4])(=[O:3])[NH2:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared by the procedures of Example 16 from sulfamoyl chloride and to 2-(3,4-dichlorophenoxy)ethanol. The tan colored solid obtained was dissolved in isopropyl ether and the solution treated with charcoal and filtered through Celite®. The filtrate was evaporated under reduced pressure and the solid residue was recrystallized from isopropyl ether to give the title compound, mp 84°-85° C., in 19% yield.
Workup
- customThe tan colored solid obtained
- filtrationfiltered through Celite®
- customThe filtrate was evaporated under reduced pressure
- customthe solid residue was recrystallized from isopropyl ether
Sources & evidence
- ORD record
- ord-05faf73ec11741949f749a017da5168e
- Source dataset
- uspto-grants-1991_06
- Patent number
- US05025031
Reaction notes
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