Methane → HCID 19108674, compound
Reaction equation
[S:1](Cl)(=[O:4])(=[O:3])[NH2:2].[CH3:6][O:7][C:8]1[CH:17]=[CH:16][CH:15]=[CH:14][C:9]=1[O:10][CH2:11][CH2:12][OH:13].C>C(Cl)Cl>[CH3:6][O:7][C:8]1[CH:17]=[CH:16][CH:15]=[CH:14][C:9]=1[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 procedure of Example 16 from sulfamoyl chloride and 2-(2-methoxyphenoxy)ethanol. The solid obtained was dissolved in 150 ml of methylene chloride, and the solution was treated with charcoal and filtered through Celite®. The filtrate was evaporated under reduced pressure and the solid residue was recrystallized from methylene chloride-petroleum ether (30°-60° C.) to give the title compound in 25% yield as a white solid, mp 102°-104° C.
Workup
- customThe solid obtained
- filtrationfiltered through Celite®
- customThe filtrate was evaporated under reduced pressure
- customthe solid residue was recrystallized from methylene chloride-petroleum ether (30°-60° C.)
Sources & evidence
- ORD record
- ord-f76839b3291744728d4cddb16ef19cf9
- Source dataset
- uspto-grants-1991_06
- Patent number
- US05025031
Reaction notes
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