88-34-6

Usage

Uses

Used in Pharmaceutical Industry:
[2,4-bis(1,1-dimethylpropyl)phenoxy]acetyl chloride is used as a reactive intermediate for the preparation of various pharmaceuticals. Its unique structure allows for the synthesis of a wide range of drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
[2,4-bis(1,1-dimethylpropyl)phenoxy]acetyl chloride is also used in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products that can improve crop yields and protect plants from pests and diseases.
Used in Organic Synthesis:
[2,4-bis(1,1-dimethylpropyl)phenoxy]acetyl chloride serves as a versatile building block in organic synthesis, enabling the creation of various organic compounds with diverse applications in different industries.
It is important to handle and store [2,4-bis(1,1-dimethylpropyl)phenoxy]acetyl chloride with proper safety precautions due to its corrosive and hazardous nature.

InChI:InChI=1/C18H27ClO2/c1-7-17(3,4)13-9-10-15(21-12-16(19)20)14(11-13)18(5,6)8-2/h9-11H,7-8,12H2,1-6H3

Upstream product

• 13402-96-5 2-(2,4-di-t-amylphenoxy)acetic acid 
• 120-95-6 2,4-di-tert-amylphenol 

Downstream Products

• 71653-91-3 (2,4-di-tert-pentyl-phenoxy)-acetic acid-[3-(4-oxo-3-phenyl-2-phenylimino-thiazolidin-5-ylidenemethyl)-phenyl ester] 
• 116671-04-6 4-[2-(2,4-di-tert-pentyl-phenoxy)-acetylamino]-2-methoxy-1-(3-oxo-3-phenyl-propionylamino)-benzene 
• 116670-71-4 4-[2-(2,4-di-tert-pentyl-phenoxy)-acetylamino]-1-methoxy-2-(3-oxo-3-phenyl-propionylamino)-benzene 
• 103325-59-3 3-[2-(2,4-di-tert-pentyl-phenoxy)-acetylamino]-benzoic acid-(5-chloro-2-hydroxy-4-methyl-anilide) 
• 858816-51-0 1-[2-(2,4-di-tert-pentyl-phenoxy)-acetylamino]-4-[3-(2-methoxy-phenyl)-3-oxo-propionylamino]-benzene 
• 50670-98-9 α-Chlor-α-<2-fluor-4-<α-(2,4-di-t-amylphenoxy)-acetylamino>-benzoyl>-2-methoxyacetanilid 
• 50670-99-0 3-Nitro-4-chlor-α-(2,4-di-t-amylphenoxy)-acetanilid 
• 50671-26-6 α-(2-Fluorbenzoyl)-5-<α-(2,4-di-t-amylphenoxy)-acetylamino>-2-methoxyacetanilid 
• 50671-04-0 α-(2-Chlorbenzoyl)-2-methoxy-5-<α-(2,4-di-t-amylphenoxy)-acetylamino>-acetanilid 
• 31188-91-7 3-[3-(2'',4''-di-tert-pentyl)phenoxyacetamido]benzoylamino-1-(2',4',6'-trichlorophenyl)-4,5-dihydropyrazol-5(1H)-one 
• 97691-99-1 2-Chloro-5-methoxy-4,4-dimethyl-3-oxo-pentanoic acid (5-{2-[2,4-bis-(1,1-dimethyl-propyl)-phenoxy]-acetylamino}-2-chloro-phenyl)-amide 
• 50671-00-6 N-(3-amino-4-chlorophenyl)-2-(2,4-di-tert-pentylphenoxy)acetamide 
• 96774-03-7 4,4-Dimethyl-3-oxo-pentanoic acid (5-{2-[2,4-bis-(1,1-dimethyl-propyl)-phenoxy]-acetylamino}-2-chloro-phenyl)-amide 
• 50671-07-3 α-(2-Fluorbenzoyl)-5-<α-(2,4-di-t-amylphenoxy)-acetylamino>-2-chloracetanilid 

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.