Sign In to Follow Application
View All Documents & Correspondence

"Process For The Preparation Of Halogenated Derivatives Of Aromatic Ethers"

Abstract: ABSTRACT PROCESS FOR THE PREPARATION OF HALOGENATED DERIVATIVES OF AROMATIC ETHERS The present invention relates to the process for the preparation of halogenated derivatives of aromatic ethers of formula I. Formula I wherein R and R’ together are an oxygen atom, and X represents a hydrogen, fluorine, chlorine, bromine or iodine.

Get Free WhatsApp Updates!
Notices, Deadlines & Correspondence

Patent Information

Application #
Filing Date
11 September 2014
Publication Number
36/2016
Publication Type
INA
Invention Field
CHEMICAL
Status
Email
veena.arora@srf.com
Parent Application
Patent Number
Legal Status
Grant Date
2020-02-07
Renewal Date

Applicants

SRF LIMITED
Block-C, Sector 45, Unicrest Building, Gurgaon, Haryana (India).

Inventors

1. Ganesan Varadharaj
SRF LIMITED, Block-C, Sector-45, Unicrest Building, Gurgaon, Haryana (India);
2. Ravichandran Poornachandran
SRF LIMITED, Block-C, Sector-45, Unicrest Building, Gurgaon, Haryana (India);
3. Sarathy Iyengar
SRF LIMITED, Block-C, Sector-45, Unicrest Building, Gurgaon, Haryana (India);
4. Seetharaman Prasanna Kumar
SRF LIMITED, Block-C, Sector-45, Unicrest Building, Gurgaon, Haryana (India);
5. Srinivasan Raguraman Tiruchy
SRF LIMITED, Block-C, Sector-45, Unicrest Building, Gurgaon, Haryana (India).
6. Anantharaman Gomathinayakam
SRF LIMITED, Block-C, Sector-45, Unicrest Building, Gurgaon, Haryana (India).
7. Rajdeep Anand
SRF LIMITED, Block-C, Sector-45, Unicrest Building, Gurgaon, Haryana (India);

Specification

PROCESS FOR THE PREPARATION OF HALOGENATED
DERIVATIVES OF AROMATIC ETHERS
Field of the invention
The present invention relates to the process for the preparation of halogenated
derivatives of aromatic ethers of Formula I.
Background of the invention
The halogenated derivatives of aromatic ethers of Formula I play an important
role as precursors for the preparation of medicaments and crop protection agents.
O
R'
R
X
X X
Formula I
wherein R and R’ together are an oxygen atom, and X represents a
hydrogen, fluorine, chlorine, bromine or iodine.
The U.S Patent No. 7,148,365 describes a process for the preparation of 5-bromo-
2,2-difluorobenzo-1,3-dioxoles by reaction of 2,2-difluorobenzo-1,3-dioxoles
with bromine in the presence of at least two Friedel-Crafts catalysts of which one
is hydrogen fluoride
The U.S Patent No. 4,895,871 describes a process of preparation of 5-bromo-2,2-
difluorobenzo-1,3-dioxoles by reaction of 2,2-difluorobenzo-1,3-dioxoles with
bromine in the presence of carbon tetrachloride and iron powder.
The processes disclosed in the listed prior art employ either toxic solvents and/or
lewis acids, however, the yield of mono bromo derivatives obtained from such
processes is substantially low. Thus, there is a need in the art to provide simple,
cost-effective and industrially scalable process for the preparation of compounds
of Formula I.
2
Object of the invention:
An object of the invention is to provide a process for the preparation of
halogenated derivatives of aromatic ethers of Formula I.
O
R'
R
X
X X
Formula I
wherein R and R’ together are an oxygen atom, and X represents a
hydrogen, fluorine, chlorine, bromine or iodine.
Summary of the Invention
The present invention provides a process for the preparation of compounds of
Formula I, comprising;
O
R'
R
X
X X
Formula I
wherein R and R’ together are an oxygen atom, and X represents a
hydrogen, fluorine, chlorine, bromine or iodine.
a) reacting compound of Formula II with the source of bromine in the
presence of hydrogen peroxide, and
O
R'
R
X
X
Formula II
wherein R and R’ together are an oxygen atom, and X represents a
hydrogen, fluorine, chlorine, bromine or iodine.
3
b) isolating compound of Formula I.
Detailed Description of the Invention
The present invention provides a process for the preparation of compounds of
Formula I, comprising;
O
R'
R
X
X X
Formula I
wherein R and R’ together are an oxygen atom, and X represents a
hydrogen, fluorine, chlorine, bromine or iodine.
a) reacting compound of Formula II with the source of bromine in the
presence of hydrogen peroxide, and
O
R'
R
X
X
Formula II
wherein R and R’ together are an oxygen atom, and X represents a
hydrogen, fluorine, chlorine, bromine or iodine.
b) isolating compound of Formula I.
The compound of Formula II may be prepared by any method known in the art,
for example, method known in U.S Patent No. 4,895,871. The bromine source
may be any alkali metal bromide with mineral acid orhydrogen bromide. The
alkali metal bromide may be selected from sodium bromide, potassium bromide
and caesium bromide.The step a) may take place in the presence of mineral acid.
The mineral acid may be selected from hydrochloric acid, nitric acid, sulfuric
acid, phosphoric acid, hydrofluoric acid,fluorosulfonic acid,chlorosulfonic acid or
mixture thereof.The step a) may be carried out in the presence or absence of
4
organic solvent. The step a) may be carried at a temperature of about -15oC to about 100oC, for example, at about 5oC to about 80oC. The step a) may be aided by stirring the contents. The step a) may take place for about 5 minutes to about 60 hours, for example, 10 minutes to about 60 hours, for example, 30 hours to about 50 hours.
The process for preparation of compound of Formula I may be carried in a continuous mode.
The compound of Formula I is isolated from step a) reaction mixture. The compound of Formula I may be isolated by filtration, layer separation, decantation, evaporation, concentration, crystallization and distillation or mixture thereof.
While the present invention has been described in terms of its specific embodiments, certain modifications and equivalents will be apparent to those skilled in the art and are intended to be included within the scope of the present invention.
Example
Process of preparation of 5-bromo-2, 2-difluoro-1, 3-benzodioxole:
A mixture of 2,2-difluoro-1,3-benzodioxole (560 g) and Hydrogen bromide(1100 g, Assay 47%) were taken in a reaction vessel fitted with cold condenser. The reaction mixture was cooled to 10°C and 30 % Hydrogen Peroxide solution (806 g) was added slowly in lot wise. Upon completion of addition, the temperature of the reaction mixture was cautiously raised to 70°C. The organic layer was separated and washed with 20 % of sodium metabisulfite and then washed with 20% of potassium bicarbonate solution. The organic layer was dried over magnesium sulfate and filtered. The filtrate was distilled under high vacuum to obtain the title compound.
Yield: 538 g

We claim:
1. A process for the preparation of compounds of Formula I, comprising;
a) reacting compound of Formula II with the source of bromine in the
presence of hydrogen peroxide, and
O
R'
R
X
X
Formula II
O
R'
R
X
X X
Formula I
wherein R and R’ together are an oxygen atom, and X represents a
hydrogen, fluorine, chlorine, bromine or iodine.
b) isolating compound of Formula I.
2. The process of claim 1, wherein bromine source of step a) is any alkali
metal bromide with mineral acid or hydrogen bromide.
3. The process of claim 2, wherein alkali metal bromide is selected from
sodium bromide, potassium bromide and caesium bromide.
4. The process of claim 2, wherein mineral acid is selected from
hydrochloric acid, nitric acid, sulfuric acid, phosphoric acid, hydrofluoric
acid, fluoro sulfonic acid, chloro sulfonic acid or mixture thereof.
5. The process of claim 1, wherein step a) is carried at a temperature of
about -15oC to about 100oC.
6. The process of claim 1, wherein compound of Formula I is isolated by
filtration, layer separation, decantation, evaporation, concentration,
crystallization and distillation or mixture thereof.

Documents

Application Documents

# Name Date
1 2611-DEL-2014-RELEVANT DOCUMENTS [26-09-2023(online)].pdf 2023-09-26
1 Form-3.pdf 2014-09-26
2 2611-DEL-2014-RELEVANT DOCUMENTS [21-09-2022(online)].pdf 2022-09-21
2 Form-2 Final.pdf 2014-09-26
3 ABSTRACT.pdf 2014-09-26
3 2611-DEL-2014-RELEVANT DOCUMENTS [22-09-2021(online)].pdf 2021-09-22
4 2611-DEL-2014-Power of Attorney-071114.pdf 2014-12-03
4 2611-DEL-2014-IntimationOfGrant07-02-2020.pdf 2020-02-07
5 2611-DEL-2014-PatentCertificate07-02-2020.pdf 2020-02-07
5 2611-DEL-2014-Correspondence-071114.pdf 2014-12-03
6 2611-del-2014-Form-1-(15-12-2014).pdf 2014-12-15
6 2611-DEL-2014-Annexure (Optional) [09-12-2019(online)].pdf 2019-12-09
7 2611-DEL-2014-PETITION UNDER RULE 137 [09-12-2019(online)]-1.pdf 2019-12-09
7 2611-del-2014-Correspondance Others-(15-12-2014).pdf 2014-12-15
8 OTHERS [11-09-2015(online)].pdf 2015-09-11
8 2611-DEL-2014-PETITION UNDER RULE 137 [09-12-2019(online)].pdf 2019-12-09
9 2611-DEL-2014-RELEVANT DOCUMENTS [09-12-2019(online)]-1.pdf 2019-12-09
9 Description(Complete) [11-09-2015(online)].pdf 2015-09-11
10 2611-DEL-2014-RELEVANT DOCUMENTS [09-12-2019(online)].pdf 2019-12-09
10 Assignment [11-09-2015(online)].pdf 2015-09-11
11 2611-DEL-2014-FER.pdf 2018-09-13
11 2611-DEL-2014-Response to office action (Mandatory) [09-12-2019(online)].pdf 2019-12-09
12 2611-DEL-2014-HearingNoticeLetter-(DateOfHearing-06-12-2019).pdf 2019-11-22
12 2611-DEL-2014-RELEVANT DOCUMENTS [13-03-2019(online)].pdf 2019-03-13
13 2611-DEL-2014-AMENDED DOCUMENTS [13-03-2019(online)].pdf 2019-03-13
13 2611-DEL-2014-OTHERS [13-03-2019(online)].pdf 2019-03-13
14 2611-DEL-2014-CLAIMS [13-03-2019(online)].pdf 2019-03-13
14 2611-DEL-2014-MARKED COPIES OF AMENDEMENTS [13-03-2019(online)].pdf 2019-03-13
15 2611-DEL-2014-CORRESPONDENCE [13-03-2019(online)].pdf 2019-03-13
15 2611-DEL-2014-FORM-26 [13-03-2019(online)].pdf 2019-03-13
16 2611-DEL-2014-FER_SER_REPLY [13-03-2019(online)].pdf 2019-03-13
16 2611-DEL-2014-FORM 13 [13-03-2019(online)].pdf 2019-03-13
17 2611-DEL-2014-FORM 13 [13-03-2019(online)].pdf 2019-03-13
17 2611-DEL-2014-FER_SER_REPLY [13-03-2019(online)].pdf 2019-03-13
18 2611-DEL-2014-CORRESPONDENCE [13-03-2019(online)].pdf 2019-03-13
18 2611-DEL-2014-FORM-26 [13-03-2019(online)].pdf 2019-03-13
19 2611-DEL-2014-CLAIMS [13-03-2019(online)].pdf 2019-03-13
19 2611-DEL-2014-MARKED COPIES OF AMENDEMENTS [13-03-2019(online)].pdf 2019-03-13
20 2611-DEL-2014-AMENDED DOCUMENTS [13-03-2019(online)].pdf 2019-03-13
20 2611-DEL-2014-OTHERS [13-03-2019(online)].pdf 2019-03-13
21 2611-DEL-2014-HearingNoticeLetter-(DateOfHearing-06-12-2019).pdf 2019-11-22
21 2611-DEL-2014-RELEVANT DOCUMENTS [13-03-2019(online)].pdf 2019-03-13
22 2611-DEL-2014-FER.pdf 2018-09-13
22 2611-DEL-2014-Response to office action (Mandatory) [09-12-2019(online)].pdf 2019-12-09
23 2611-DEL-2014-RELEVANT DOCUMENTS [09-12-2019(online)].pdf 2019-12-09
23 Assignment [11-09-2015(online)].pdf 2015-09-11
24 Description(Complete) [11-09-2015(online)].pdf 2015-09-11
24 2611-DEL-2014-RELEVANT DOCUMENTS [09-12-2019(online)]-1.pdf 2019-12-09
25 OTHERS [11-09-2015(online)].pdf 2015-09-11
25 2611-DEL-2014-PETITION UNDER RULE 137 [09-12-2019(online)].pdf 2019-12-09
26 2611-DEL-2014-PETITION UNDER RULE 137 [09-12-2019(online)]-1.pdf 2019-12-09
26 2611-del-2014-Correspondance Others-(15-12-2014).pdf 2014-12-15
27 2611-del-2014-Form-1-(15-12-2014).pdf 2014-12-15
27 2611-DEL-2014-Annexure (Optional) [09-12-2019(online)].pdf 2019-12-09
28 2611-DEL-2014-PatentCertificate07-02-2020.pdf 2020-02-07
28 2611-DEL-2014-Correspondence-071114.pdf 2014-12-03
29 2611-DEL-2014-Power of Attorney-071114.pdf 2014-12-03
29 2611-DEL-2014-IntimationOfGrant07-02-2020.pdf 2020-02-07
30 ABSTRACT.pdf 2014-09-26
30 2611-DEL-2014-RELEVANT DOCUMENTS [22-09-2021(online)].pdf 2021-09-22
31 2611-DEL-2014-RELEVANT DOCUMENTS [21-09-2022(online)].pdf 2022-09-21
31 Form-2 Final.pdf 2014-09-26
32 2611-DEL-2014-RELEVANT DOCUMENTS [26-09-2023(online)].pdf 2023-09-26
32 Form-3.pdf 2014-09-26

Search Strategy

1 2611_del_2014patseersearchstrategy_21-03-2018.pdf
1 googlesearch_21-03-2018.pdf
2 googlesearch2_21-03-2018.pdf
3 2611_del_2014patseersearchstrategy_21-03-2018.pdf
3 googlesearch_21-03-2018.pdf

ERegister / Renewals

3rd: 05 May 2020

From 11/09/2016 - To 11/09/2017

4th: 05 May 2020

From 11/09/2017 - To 11/09/2018

5th: 05 May 2020

From 11/09/2018 - To 11/09/2019

6th: 05 May 2020

From 11/09/2019 - To 11/09/2020

7th: 05 May 2020

From 11/09/2020 - To 11/09/2021

8th: 01 Sep 2021

From 11/09/2021 - To 11/09/2022

9th: 02 Sep 2022

From 11/09/2022 - To 11/09/2023

10th: 11 Sep 2023

From 11/09/2023 - To 11/09/2024