4-t-Butylbenzenesulfonyl chloride → Benzenesulfonamide
Reaction equation
C([C:5]1[CH:10]=[CH:9][C:8]([S:11](Cl)(=[O:13])=[O:12])=[CH:7][CH:6]=1)(C)(C)C.[N:15]1C=CC=CC=1.C1(C)C=CC=CC=1>>[C:8]1([S:11]([NH2:15])(=[O:13])=[O:12])[CH:9]=[CH:10][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
Reaction with p-tert-butylbenzenesulphonyl chloride in pyridine/toluene at room temperature yielded pure 4-tert-butyl-N-[3-(2-tetrahydropyranyloxyethoxy)-2-methoxy-phenoxy)-phenyl]-benzenesulphonamide. MS: Mt /e=555.
Sources & evidence
- ORD record
- ord-18a535080f7247fd8430b79d0b11a6e1
- Source dataset
- uspto-grants-1999_10
- Patent number
- US05962682
Reaction notes
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