40567-16-6

Usage

Uses

Used in Pharmaceutical Industry:
2-[2,4-bis(1,1-dimethylpropyl)phenoxy]butyryl chloride is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique structure allows for the creation of novel compounds with potential therapeutic applications, contributing to the advancement of medicine.
Used in Agrochemical Industry:
In the agrochemical sector, 2-[2,4-bis(1,1-dimethylpropyl)phenoxy]butyryl chloride serves as a key component in the synthesis of agrochemicals. Its reactivity and functional groups enable the production of compounds with pesticidal or herbicidal properties, aiding in crop protection and yield enhancement.
Used in Research and Development:
2-[2,4-bis(1,1-dimethylpropyl)phenoxy]butyryl chloride is employed as a versatile building block in the research and development of new chemical compounds. Its reactivity and structural features make it a valuable tool for chemists exploring novel synthetic pathways and creating innovative molecules with diverse applications.

InChI:InChI=1/C20H31ClO2/c1-8-16(18(21)22)23-17-12-11-14(19(4,5)9-2)13-15(17)20(6,7)10-3/h11-13,16H,8-10H2,1-7H3

Upstream product

• 13403-01-5 2-(2,4-di-tert-pentylphenoxy)butyric acid 

Downstream Products

• 31037-84-0 2-(2,4-di-tert-pentyl-phenoxy)-butyric acid-(3,5-dichloro-2-hydroxy-4-methyl-anilide) 
• 94109-73-6 {4-[2-(2,4-di-tert-pentyl-phenoxy)-butyrylamino]-phenoxy}-acetic acid-(3,5-dichloro-2-hydroxy-4-methyl-anilide) 
• 38881-04-8 2-[2,4-Bis-(1,1-dimethyl-propyl)-phenoxy]-N-(2-hydroxy-4-nitro-phenyl)-butyramide 
• 38881-05-9 N-(4-Amino-2-hydroxy-phenyl)-2-[2,4-bis-(1,1-dimethyl-propyl)-phenoxy]-butyramide 
• 102580-11-0 4-[α-(2,4-ditert.-pentylphenoxy)-butyroyl]-6-benzyloxy-7-nitro-1,4-benzoxazine-3-one 
• 1219449-11-2 C₂₂H₃₄N₄O₂ 

Relevant academic research and scientific papers

Process for producing aromatic amide compounds

There is disclosed a process for producing an aromatic amide compound of the general formula (4), including the steps of subjecting an o-nitrophenol compound of the general formula (1) to catalytic reduction in acetone or an aromatic hydrocarbon solvent under the presence of a nickel catalyst to give an o-aminophenol compound of the general formula (2); and (b) subjecting the o-aminophenol compound of the general formula (2) to condensation with an acid chloride compound having a sulfur content of 0.5% or less, based on the weight of the acid chloride compound, of the general formula (3) in acetone or an aromatic hydrocarbon solvent under an atmosphere of an inert gas having an oxygen concentration of 1% or less. The acid chloride compound having a sulfur content of 0.5% or less, based on the weight of the acid chloride compound, of the general formula (3) may be obtained by allowing a carboxylic acid compound of the general formula (5) to react with thionyl chloride and by concentrating the reaction mixture. Also disclosed is another process for producing an aromatic amide compound of the general formula (4), including the step of subjecting an o-aminophenol hydrochloride salt of the general formula (6) to condensation with an acid chloride compound having a sulfur content of 0.8% or less, based on the weight of the acid chloride compound, of the general formula (3) in an inert solvent.