1H-Pyrazole-4-carboxylic acid, 5-chloro-1,3-dimethyl-, 4-[2-chloro-3-[(5-methyl-2-oxo-1,3,4-oxadiazol-3(2H)-yl)methyl]-4-(methylsulfonyl)benzoyl]-3-cyclopropyl-1-methyl-1H-pyrazol-5-yl ester

Prochlorosulfone is synthesised through a multi-step condensation process. Commercial production begins with the preparation of a substituted benzoyl chloride, which is reacted with a methylsulfonyl group and a chloro-substituted aromatic ring. This intermediate is then coupled with heterocyclic components, specifically a pyrazole derivative and an oxadiazolone fragment, using controlled acylation and esterification reactions. The process requires precise temperature and pH control to maintain stereochemistry (typically the (1R,3R)-cyclopropyl configuration) for optimal herbicidal activity. After assembly of the full molecule, the product undergoes purification and crystallisation to achieve technical-grade purity suitable for formulation.

Bleaching: inhibition of 4-hydroxyphenyl-pyruvate-dioxygenase.

Herbicide