Process for the preparation of aromatic sulfonyl chlorides
AssigneeHoechst Aktiengesellschaft
InventorsMichael Meier, Wolfgang Tronich
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AssigneeHoechst Aktiengesellschaft
InventorsMichael Meier, Wolfgang Tronich
Estimating the term…
A process for the preparation of aromatic sulfonyl chlorides of the formula I ##STR1## in which R.sub.1, R.sub.2 and R.sub.3 are identical or different and are hydrogen, fluorine, chlorine, bromine or iodine atoms, alkyl(C.sub.1 -C.sub.4), acetamido, nitro or carboxyl groups, or R.sub.1 and R.sub.2 together form an aromatic or heteroaromatic ring having 5 or 6 ring members, which can be substituted by fluorine, chlorine, bromine or iodine atoms, alkyl(C.sub.1 -C.sub.4), acetamido, nitro or carboxyl groups, by reaction of aromatic compounds of the formula II ##STR2## in which R.sub.1, R.sub.2 and R.sub.3 have the abovementioned meanings, with chlorosulfonic acid in excess or with chlorosulfonic acid or oleum and thionyl chloride, by reacting in the presence of sulfamic acid as a catalyst.
A process for the preparation of aromatic sulfonyl chlorides of the formula I ##STR5## in which R.sub.1, R.sub.2 and R.sub.3 are identical or different and are hydrogen, fluorine, chlorine, bromine or iodine atoms, alkyl (C.sub.1 -C.sub.4), acetamido, nitro or carboxyl groups, or R.sub.1 and R.sub.2 together form an aromatic ring having 5 to 6 ring members or form an oxazolone ring which comprises reacting aromatic compounds of the formula II ##STR6## in which R.sub.1, R.sub.2 and R.sub.3 have the abovementioned meanings, with chlorosulfonic acid in excess or with chlorosulfonic acid or oleum and thionyl chloride in the presence of about 0.1 to about 20% by weight of sulfamic acid relative to the aromatic compound of said formula II as a catalyst at a temperature in the range of from -10 to 150.degree. C.
Dependencies are inferred from the claim text.