Prepn of etofenprox as pesticide
A technology for etherethrin and insecticide, which is applied in the field of chemical preparation of the pesticide etherethrin, can solve the problems of harsh reaction conditions, high cost of raw materials, and difficulty in industrialization.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0013] Add (industrial grade) 304 grams (2 mol) of p-tert-butylphenol and 229 grams (2.2 mol) of acid anhydride into a 1000 ml three-necked reaction flask, add 1 mL of inorganic acid, heat and stir, heat up to 130 ° C, react for 8 hours, and reduce The by-product acetic acid and unreacted acetic anhydride were steamed under pressure, the kettle liquid was washed to neutrality, and the layers were separated, and the oil phase was dried to obtain p-tert-butylacetophenone, weighing 384 grams, and the content after analysis was 97%. The rate is 97%.
[0014] Add the prepared p-tert-butylacetophenone (1.94mol) into a 1000ml three-necked reaction flask, add 2g of azobisisobutyronitrile as an initiator, add 450mL of carbon tetrachloride, heat and stir, heat up to 80°C and reflux, Chlorine gas was passed for 3 hours, and the whole reaction was irradiated with a fluorescent lamp. The reaction solution was washed with 600mL of 3% sodium sulfite aqueous solution and separated into layer...
Embodiment 2
[0018] A total of 83.9 grams of unused [4-(2-chloro-1,1-dimethylethyl)phenyl] acetate obtained from the reaction in Example 1 has a content of 98%. A total of 0.364mol of the above-mentioned raw materials, as well as 108 grams (0.9mol) of bromoethane and 82.5 grams of KOH were added to a 500 ml three-necked reaction flask, heated and stirred, and 2.1 grams of benzyltriethylammonium chloride could be dropped in. The reaction temperature was 35 ~45°C, the reaction time is 2 hours, the reaction solution is washed several times with 150mL water and separated, the liquid phase is the product 1-chloro-2-(4-ethoxyphenyl)-2-methylpropane 77.8 grams , crude product content 80.6%, yield 81.3%.
[0019] Add 39.4 grams (0.15mol) of 1-chloro-2-(4-ethoxyphenyl)-2-methylpropane, 33.8 grams (0.16mol) of sodium m-phenoxybenzyloxide into a 250 ml three-necked reaction flask. ), 0.38 grams of tetraethylammonium bromide, 150 milliliters of DMF, heated and stirred, heated up to 120 ° C for 8 hour...
Embodiment 3
[0021] Add 38.4 grams (0.15mol) of the remaining 1-chloro-2-(4-ethoxyphenyl)-2-methylpropane prepared in Example 3 to a 250 ml three-necked reaction flask, 33.8 m-phenoxybenzyl sodium gram (0.16mol), 0.38 gram of tetraethylammonium bromide, 150 milliliters of DMF, heated and stirred, heated up to 140 ℃ and reacted for 16 hours. Purified to obtain 34.1 grams with a content of 82.3%, and a yield of 49.7%.
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com