107960-33-8

Upstream product

• 1940-57-4 9H-fluoren-9-yl bromide 
• 107960-26-9 C₉H₇N₂O₂^(1-)*Ag⁽¹⁺⁾ 
• 22364-68-7 2-tolylmethylnitrile 

Downstream Products

• 133409-72-0 methyl (E)-2-[2-(bromomethyl)phenyl]-2-(methoxyimino)acetate 
• 120974-97-2 methyl-(E)-2-(2-tolyl)-2-methoxyiminoacetate 
• 143390-89-0 methyl (E)-2-methoxyimino-2-[2-(o-tolyloxymethyl)phenyl]acetate 
• 156581-21-4 (E)-2-methyl-α-methoxyiminophenylacetonitrile 
• 159731-22-3 (Z)-2-methyl-α-methoxyiminophenylacetonitrile 
• 52042-86-1 C₁₇H₁₁Cl₃FN₃O₂S 
• 52042-89-4 C₁₇H₁₂Cl₂FN₃O₂S 

Relevant academic research and scientific papers

Green synthetic method of kresoxim-methyl

The invention belongs to the technical field of fine chemical engineering, and particularly relates to a green synthetic method of kresoxim-methyl. The method comprises the following steps: carrying out nitrous nitrification by using 2-methylbenzyl cyanide as an initial raw material, carrying out methylation, carrying out hydrolytic methylation or hydrolytic esterification, carrying out bromination and carrying out an etherification reaction to obtain the high-content kresoxim-methyl. The method provided by the invention has a short reaction period, a high conversion rate, and excellent product quality, changes the defect that high-concentration hydrochloric acid gas is used for preparation in a traditional process, and has the advantages of simple operation steps, simple equipment, low energy consumption, a short period, high productivity and environmental protection.

Cu-Mediated Stereoselective [4+2] Annulation between N-Hydroxybenzimidoyl Cyanide and Norbornene

A Cu-mediated stereoselective [4+2] annulation between N-hydroxybenzimidoyl cyanides and norbornene (NBE) has been developed for the synthesis of 4H-1,2-oxazin-4-ones. The reaction proceeds through sequentially forming C-O/C-C bonds. The advantage of this reaction includes high stereoselectivity, excellent yields, as well as simple and mild reaction conditions. A total of 26 examples are presented along with some control experiments.

Reaction of the Silver Salts of Arylnitroacetonitriles with 9-Bromofluorene. Synthesis of 9-(α-Cyanoarylidene)fluorenes

The silver salts 1a-d react with 9-bromofluorene to give both C- and O-alkylated products 2 and 3.The latter decompose to yield 9-fluorenone and the α-cyanooximes 5.The products 2 upon treatment with NaOH/EtOH eliminate HNO2 to afford 9-(α-cyanoarylidene)fluorenes 4 in 80percent yield. 9-Chloro-9-phenylfluorene reacts with salt 1a to give only C-alkylated product 6 in 70percent yield.