Efficient synthesis of optically active herbicide (S)-metolachlor via reductive ring opening of 2-methoxymethylaziridine

TitleEfficient synthesis of optically active herbicide (S)-metolachlor via reductive ring opening of 2-methoxymethylaziridine
Publication TypeJournal Article
Year of Publication2023
AuthorsNalla, V, Mujahid, M, Sasikumar, M, Mujumdar, P, Muthukrishnan, M
JournalArkivoc
Date PublishedJUL
Type of ArticleArticle
ISSN1551-7004
KeywordsAziridine, Epoxide, Epoxide ring opening, herbicide synthesis, Metolachlor
Abstract

An efficient synthesis of a well known chiral herbicide, (S)-metolachlor has been described using 2methoxymethylaziridine ring formation and reductive ring opening as key steps using commercially available (R)-epichlorohydrin. The present protocol delivers the required enantiomer of metolachlor in overall yield of 50.8% and high enantiopurity (>99%).

DOI10.24820/ark.5550190.p011.954
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

0.9

Divison category: 
Organic Chemistry
Database: 
Web of Science (WoS)

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