Chlorosulfonic acid → Chlorobenzene sulfochloride
Reaction equation
CCC(CCCCC(NC(C(NC(C(NC(C(NC1C(=O)NC(CCN)C(=O)NC(C[C:67]2[CH:72]=[CH:71][CH:70]=[CH:69][CH:68]=2)C(=O)NC(CC(C)C)C(=O)NC(CCN)C(=O)NC(CCN)C(=O)NC(C(O)C)C(=O)NCC1)=O)CCN)=O)C(O)C)=O)CCN)=O)C.OS(O)(=O)=O.[Cl:91][S:92]([OH:95])(=[O:94])=[O:93]>O>[S:92]([Cl:91])([OH:95])(=[O:94])=[O:93].[Cl:91][C:67]1[CH:72]=[CH:71][CH:70]=[CH:69][CH:68]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
adding said reaction mixture to water or diluted sufuric acid to decompose said excess chlorosulfonic acid and to form a chlorobenzene sulfochloride layer and a sulfuric acid layer having a sulfuric acid concentration of from 60 to 90% after completion of said decomposition, said decomposition being carried out at a temperature of from 50° to 85° C., and driving off remaining hydrogen chloride from the system; and
Workup
- additionadding
Sources & evidence
- ORD record
- ord-5e5e78ad79d84ccfb83c43778189e3ab
- Source dataset
- uspto-grants-1987_05
- Patent number
- US04666637
Reaction notes
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