WO2023223105 - A PROCESS OF PREPARATION OF 3'-(TRIFLUOROMETHYL)ACETOPHENONE (TFMAP)

National phase entry is expected:
Publication Number WO/2023/223105
Publication Date 23.11.2023
International Application No. PCT/IB2023/051349
International Filing Date 15.02.2023
Title **
[English] A PROCESS OF PREPARATION OF 3'-(TRIFLUOROMETHYL)ACETOPHENONE (TFMAP)
[French] PROCÉDÉ DE PRÉPARATION DE 3 '- (TRIFLUOROMÉTHYLE) ACÉTOPHÉNONE (TFMAP)
Applicants **
DEEPAK NITRITE LIMITED
Inventors
ISMAILI, Aminmahamad N
PATIL, Vilas
MANSURI, Javedhusen K
Priority Data
202221028493   18.05.2022   IN
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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting2074
EPO Filing, Examination, Granting11708
Japan Filing, Examination, Granting2167
South Korea Filing, Examination, Granting2005
USA Filing, Examination, Granting4740
MasterCard Visa
Total: 22,694

The term for entry into the National Phase has expired. This quotation is for informational purposes only

Abstract[English] Disclosed is a system (100) and process (300) for preparation of 3'-(Trifluoromethyl) acetophenone (TFMAP), wherein disclosed TFMAP provides appearance ranging from colourless to orange liquid, purity in the range of 99-99.9%, and yield in the range of 60-90%. The process (300) for preparation of the TFMAP include preparation of a diazo solution from reacting 3-aminobenzotrifluoride and sulfuric acid, followed by lot-wise addition of diazo solution with acetaldoxime to obtain 3'- (Trifluoromethyl)acetophenone oxime, which is further treated with 30% HCl solution and undergo distillation to obtain 3'-(Trifluoromethyl) acetophenone having enhanced yield and purity.[French] Sont divulgués un système (100) et un procédé (300) pour la préparation de 3 '- (trifluorométhyle) acétophénone (TFMAP), le TFMAP divulgué fournissant un aspect allant d'un liquide incolore à orange, une pureté dans la plage de 99 à 99,9 %, et un rendement dans la plage de 60 à 90 %. Le procédé (300) pour la préparation du TFMAP comprend la préparation d'une solution diazo à partir de la réaction de 3-aminobenzotrifluorure et d'acide sulfurique, suivie d'une addition par lots de solution diazo avec de l'acétaldoxime pour obtenir l'oxime de 3 '- (trifluorométhyle) acétophénone, qui est en outre traitée avec une solution HCl à 30 % et subit une distillation pour obtenir de la 3 '- (trifluorométhyle) acétophénone ayant un rendement et une pureté améliorés.

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