<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>31(3)</volume><submitter>Chen W</submitter><pubmed_abstract>Control of process-related impurities is of critical importance for developing an efficient and suitable synthetic process of an active pharmaceutical ingredient. In the study of a key intermediate of silodosin (KIS), two process-related impurities including the benzaldehyde impurity (BAI) and indole impurity (IDI) were prepared and fully characterized to determine their downstream fate. Under optimized conditions, BAI was formed in a yield of ~48% by treating KIS with 10% hydrogen peroxide at 60 °C. Interestingly, BAI would not be expected to be the major product under the apparent Baeyer-Villiger oxidative condition. Furthermore, by adding 20 mM FeCl&lt;sub>3&lt;/sub> into the above 10% hydrogen peroxide solution, IDI became the major product in a yield of ~43% under this Fenton reaction-like </pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pagination>462</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12898569</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Preparation of Two Process-Related Impurities of a Key Intermediate of Silodosin Under Baeyer-Villiger and Fenton Conditions.</pubmed_title><pmcid>PMC12898569</pmcid><pubmed_authors>Xi J</pubmed_authors><pubmed_authors>Zhou Q</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Bai Z</pubmed_authors><pubmed_authors>Jin J</pubmed_authors><pubmed_authors>Li M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Preparation of Two Process-Related Impurities of a Key Intermediate of Silodosin Under Baeyer-Villiger and Fenton Conditions.</name><description>Control of process-related impurities is of critical importance for developing an efficient and suitable synthetic process of an active pharmaceutical ingredient. In the study of a key intermediate of silodosin (KIS), two process-related impurities including the benzaldehyde impurity (BAI) and indole impurity (IDI) were prepared and fully characterized to determine their downstream fate. Under optimized conditions, BAI was formed in a yield of ~48% by treating KIS with 10% hydrogen peroxide at 60 °C. Interestingly, BAI would not be expected to be the major product under the apparent Baeyer-Villiger oxidative condition. Furthermore, by adding 20 mM FeCl&lt;sub>3&lt;/sub> into the above 10% hydrogen peroxide solution, IDI became the major product in a yield of ~43% under this Fenton reaction-like </description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-09T13:12:01.426Z</modification><creation>2026-07-09T13:09:13.422Z</creation></dates><accession>S-EPMC12898569</accession><cross_references><pubmed>41683439</pubmed><doi>10.3390/molecules31030462</doi></cross_references></HashMap>