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Last updated January 31, 2026
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Aromatic acyl and ether substitution: BASFRecent Research Landscape

Inefficient halogenation and alkylation steps in fine chemical production lead to low yields and high waste. These processes control specific substitution pathways to ensure high-purity fluorinated intermediates.

What technical problems is BASF addressing in Aromatic acyl and ether substitution?

Low chemical synthesis yields

(19)evidences

Inefficient formation of specific isomers during complex aromatic substitution. Improving selectivity reduces byproduct waste and purification complexity in herbicide and pharmaceutical precursor production.

Low chemical synthesis yields

(12)evidences

Inefficient substitution patterns and byproduct formation during aromatic acylation and etherification. Improving precision reduces waste and purification costs.

Inefficient aromatic functionalization pathways

(11)evidences

Conventional aromatic substitution often suffers from poor yield and lack of positional control in complex aryl structures. Achieving precise functionalization at specific carbon sites enables the production of high-purity pharmaceutical intermediates.