2-氯-4-氟-5-硝基苯甲酸的制备方法

By using the nitration-hydrolysis reaction of 2-chloro-4-fluorobenzonitrile with sulfuric acid and nitric acid, the problems of poor selectivity and high cost in the existing technology have been solved, and the synthesis of 2-chloro-4-fluoro-5-nitrobenzoic acid with high selectivity has been achieved, which is suitable for industrial production.

CN118955293BActive Publication Date: 2026-07-17NUTRICHEM LAB CO LTD

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
NUTRICHEM LAB CO LTD
Filing Date
2024-07-26
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Existing technologies exhibit poor selectivity in the synthesis of 2-chloro-4-fluoro-5-nitrobenzoic acid, generating a 3-position mononitrated isomer, and are costly and difficult to effectively separate and purify.

Method used

A one-pot synthesis of 2-chloro-4-fluoro-5-nitrobenzoic acid was achieved by nitrification of 2-chloro-4-fluorobenzonitrile with sulfuric acid and nitric acid, followed by hydrolysis. By controlling the reaction conditions and solvent ratio, the formation of the 3-position mononitrated isomer was avoided.

Benefits of technology

It significantly improves the selectivity of 2-chloro-4-fluoro-5-nitrobenzoic acid, hardly generates the 3-position mononitrated isomer, simplifies the purification process, saves recrystallization solvent, is easy to operate, and is suitable for industrial production.

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Abstract

本发明涉及农药领域,公开了一种2‑氯‑4‑氟‑5‑硝基苯甲酸的制备方法。本发明的2‑氯‑4‑氟‑5‑硝基苯甲酸的制备方法包括:1)使2‑氯‑4‑氟苯腈与硫酸和硝酸进行硝化反应,得到硝化反应产物的步骤;2)使步骤1)得到的硝化反应产物进行水解反应的步骤。根据本发明的方法,其选择性好。
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