6102-15-4

Usage

Uses

Used in Organic Synthesis:
4-Carbethoxy-3,5-dimethyl-2-cyclohexene-1-one is used as a key intermediate in organic synthesis for its ability to participate in various chemical reactions, facilitating the creation of a diverse range of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Carbethoxy-3,5-dimethyl-2-cyclohexene-1-one is used as a building block for the development of new pharmaceutical compounds. Its unique structure and reactivity contribute to the synthesis of potential drug candidates with specific therapeutic properties.
Used in Agrochemical Industry:
4-Carbethoxy-3,5-dimethyl-2-cyclohexene-1-one is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical properties allow for the development of effective compounds that can be used in agricultural applications to protect crops and enhance yield.
Synthesis Methods:
4-Carbethoxy-3,5-dimethyl-2-cyclohexene-1-one can be synthesized through various methods, including the Claisen condensation reaction and the Friedel-Crafts acylation reaction. These methods provide efficient pathways to produce the compound in a controlled and scalable manner, ensuring its availability for diverse applications across different industries.

InChI:InChI=1/C11H16O3/c1-4-14-11(13)10-7(2)5-9(12)6-8(10)3/h5,8,10H,4,6H2,1-3H3

Upstream product

• 141-97-9 ethyl acetoacetate 
• 74-86-2 acetylene 
• 123-63-7 paracetaldehyde 
• 15301-37-8 3-ethoxycarbonyl-3-penten-2-one 
• 75-07-0 acetaldehyde 

Downstream Products

• 93445-51-3 3-butyl-2,6-dimethyl-4-oxo-cyclohex-2-enecarboxylic acid ethyl ester 
• 100667-93-4 ethyl 2,6-dimethyl-4-methoxycyclohexa-1,3-dienecarboxylate 
• 93445-22-8 2-ethyl-3,5-dimethyl-cyclohex-2-enone 
• 93445-26-2 2-butyl-3,5-dimethyl-cyclohex-2-enone 
• 2320-30-1 3,5-dimethylcyclohexanone 
• 5441-52-1 3,5-dimethylcyclohexan-1-ol 
• 91157-78-7 (1α,2ξ,6β)-(+/-)-Ethyl 2-Ethenyl-2,6-dimethyl-4-oxocyclohexanecarboxylate 
• 139387-18-1 ethyl cis,cis-2,6-dimethylcyclohexan-4-one-1-carboxylate 
• 91157-78-7 (1α,2β,6α)-(+/-)-Ethyl 2-Ethenyl-2,6-dimethyl-4-oxocyclohexanecarboxylate 
• 1097633-92-5 3-diazo-2,6-dimethyl-4-oxo-cyclohex-1-enecarboxylic acid ethyl ester 
• 928312-75-8 4-allyloxy-2,6-dimethyl-3-phenylamino-benzoic acid ethyl ester 
• 67543-92-4 3,5-dimethyl-cyclohex-2-enone oxime 
• 75056-98-3 ethyl 4-hydroxy-2,6-dimethyl benzoate 

Relevant academic research and scientific papers

Preparation method of cis, cis-3, 5-dimethyl-1-cyclohexanol

The invention belongs to the field of chemistry, and discloses a synthesis method of a cis, cis-3, 5-dimethyl-1-cyclohexanol compound shown as a formula (I). Acetaldehyde and ethyl acetoacetate are used as raw materials, and cis, cis-3, 5-dimethyl-1-cyclohexanol is synthesized by a series of reactions such as knoevenagel condensation, hydrolysis, decarboxylation, hydrogenation reduction, reduction, acylating chlorination, hydrolysis and the like. The raw materials and auxiliary materials of the route are simple and easily available, the reaction conditions are mild, the operation is simple andconvenient, the synthesis cost is low, and the obtained product has high chiral purity (the product/isomer ratio is 30: 1-100: 1) and is suitable for large-scale production.

Role of Ring Ortho Substituents on the Configuration of Carotenoid Polyene Chains

The 9-(Z)-configuration was exclusively obtained in the carotenoid polyene chain irrespective of olefination and disconnection methods for terminal ortho-unsubstituted benzene rings. The 2,6-dimethyl substituents in the terminal rings secure an all-(E)-po

High-yielding synthesis of Nefopam analogues (functionalized benzoxazocines) by sequential one-pot cascade operations

An efficient amine-/ruthenium-catalyzed three-step process for the synthesis of Nefopam analogues was achieved through combinations of cascade enamine amination/iso-aromatization/allylation and diene or enyne metathesis as key steps starting from functionalized Hagemann's esters. In this communication, we discovered the application of ruthenium-catalysis on olefins containing free amines without in situ formation of salts.

Organocatalytic cascade reactions based on push-pull dienamine platform: Synthesis of highly substituted anilines

(Chemical Equation Presented) A practical and novel one-pot organocatalytic selective process for the cascade synthesis of highly substituted o-hydroxydiary lamines and o-pyrrolidin-1-yldiarylamines is reported. Direct combination of amine-catalyzed cascade Knoevenagel/Michael/aldol condensation/decarboxylation and cascade enamine amination/isoaromatization of alkyl acetoacetates, aldehydes, and nitrosoarenes furnished the highly functionalized anilines with high yields.