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A Novel Cobalt Catalyst For Organic Reactions And Process Thereof

Abstract: There are many benefits to organometallic catalysis, especially in 5 homogeneous catalysis for C(sp2)-H bond activation and new C-C bond formation reactions. These catalysts, which are mainly transition metal complexes with organic ligands, are very reactive and selective, which increases the range and effectiveness of different synthetic transformations. Their capacity to activate C-H 10 bonds under mild reaction conditions is a key advantage as it allows for the direct C-H alkYlation of aryl ketones without the need for transient functional groups. This reduces utilization of chemicals, cost and energy used in addition to streamlining synthetic routes. Furthermore, complex molecular architectures with high stereo- and 15 regioselectivity may be formed with the help of organometallic homogenous catalysts, making precise synthesis of complex molecules possible. The present catalyst is easy to use, industrially scalable, recyclable, and provides excellent yields of C-H a!kYlated products from nonactivated alkYl halides. The reported methods 20 need the use of excess (2-6 equivalent) of alkYl halides but this catalyst performs the catalytic reaction in the stoichiometric quantities of aryl ketone and alkYl halides.

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Notices, Deadlines & Correspondence

Patent Information

Application #
Filing Date
10 April 2024
Publication Number
44/2025
Publication Type
INA
Invention Field
CHEMICAL
Status
Email
Parent Application

Applicants

ASHOKA UNIVERSITY
PLOT NO.2, RAJIV GANDHI EDUCATION CITY, NATIONAL CAPITAL REGION P.O. RAI, SONIPAT, HARYANA-131029, INDIA

Inventors

1. PROF. VIDYA DNYANESHWAR AVASARE
DEPARTMENT OF CHEMISTRY, ASHOKA UNIVERSITY, PLOT NO.2, RAJIV GANDHI EDUCATION CITY, NATIONAL CAPITAL REGION P.O. RAI SONIPAT-131029 INDIA

Specification

TECHNICAL FIELD
[001] The present invention relates to a homogeneous cobalt
catalyst, TJ3-fluorenyl-(p2-hydoxy) cobalt(II) dimer or [Co(p2-0H)-(TJ3-
Fluorenyl)]2 for room temperature C-H alkylation of aryl ketones
5 with alkyl halides reactions. The catalyst is industrially scalable,
easy to use and cost effective.
[002] Organometallic catalysis is a type of catalysis where chemical
reactions are· sped up by using organometallic molecules.
Organometallic catalysts are made entirely of metals connected to
10 carbon and other elements that are frequently found in
organometallic compounds, in contrast to conventional metal-based
catalysts. These catalysts may catalyze a variety of transformations
in organic synthesis like C-C, C-N, C-0, C-S bond formation
reactions etc organometallic catalysis is a popular strategy in
15 contemporary synthetic chemistry because it has a number of
benefits, such as low reaction conditions, high selectivity, and
environmental friendliness.
[003] Catalysts accelerate chemical reactions by providing an
altemative reaction pathway with lower activation energy, allowing
20 reactions to proceed more rapidly than they would without the
catalyst. They may promote specific pathways or products in a
reaction, enhancing selectivity and reducing the formation of
unwanted by-products. By lowering the activation energy required
for a reaction, catalysts enable reactions to occur at lower
25 temperatures and pressures, leading to energy savings and milder
reaction conditions. They enable atom economy and achieve an
excellent yield of products, thereby improving the overall efficiency
of the reaction process. Many catalysts are compatible with green
-2-

chemistry principles, such as the use of renewable resources, nontoxic
reagents, and solvent-free conditions, contributing to more
sustainable chemical processes. Some catalysts may be recovered
and reused multiple times without losing their activity, reducing
5 costs

Documents

Application Documents

# Name Date
1 202411029064-Form 5-100424.pdf 2024-04-10
2 202411029064-Form 3-100424.pdf 2024-04-10
3 202411029064-Form 28-100424.pdf 2024-04-10
4 202411029064-Form 2-100424.pdf 2024-04-10
5 202411029064-Form 1-100424.pdf 2024-04-10
6 202411029064-FORM28 [09-12-2024(online)].pdf 2024-12-09
7 202411029064-FORM-26 [09-12-2024(online)].pdf 2024-12-09
8 202411029064-Covering Letter [09-12-2024(online)].pdf 2024-12-09