# US 2014/0194630 A1 · Process for synthesis of fipronil

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- Number: US 2014/0194630 A1
- Document ID: US20140194630A1
- Status: Published application
- Kind: A1
- Application number: 14/122,721
- Filed: 2011-12-15
- Published: 2014-07-10
- Earliest claimed: 2011-05-30
- Inventors: Keki Hormusji Gharda
- Web page: https://patentgrep.com/patent/US20140194630A1

## CPC

- C07D 231/44: Oxygen and nitrogen or sulfur and nitrogen atoms
- C07D: HETEROCYCLIC COMPOUNDS (macromolecular compounds C08)

## Abstract

A process for preparation of Fipronil (i.e. 5-amino-1-(2, 6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoro-methylsulphinyl-pyrazole) is provided, which comprises oxidizing 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-tri-fluoromethylthio-pyrazole with sulfuric acid and hydrogen peroxide as oxidizing agent in the presence of a solvent such as ethylene dichloride, chlorobenzene.

## Claims

### Claim 1

A process for preparing fipronil, said process comprising the following steps:
a. oxidizing, in a solvent selected from the group consisting of ethylene dichloride, methylene dichloride, carbon tetrachloride, chloroform, dibromoethane, bromobenzene, chlorobenzene and ortho-dichlorobenzene, a reactant mixture containing a compound 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoro methyl thio-pyrazole of formula II and concentrated sulfuric acid having concentration in the range of 75% to 98% w/w, with hydrogen peroxide having concentration in the range 40 to 70% w/w, at a temperature in the range of -10° C. to 40° C. to obtain an oxidized product mixture;
b. quenching said product mixture with water at a temperature in the range of 10 to 25° C.;
c. heating the quenched product mixture at a temperature in the range of 60 to 70° C. to obtain a biphasic system containing an aqueous phase containing sulphuric acid and an organic phase containing the oxidized product;
d. isolating said organic phase by separating the aqueous phase;
e. neutralizing the isolated organic phase containing the oxidized product to obtain crude fipronil; and
f. crystallizing the crude fipronil to obtain crystallized fipronil.

### Claim 2 (depends on 1)

The process as claimed in claim 1, wherein the amount of the hydrogen peroxide used is in the range of 0.9 moles to 1.6 moles per mole of the compound II.

### Claim 3 (depends on 1)

The process as claimed in claim 1, wherein the amount of the solvent used is 100 to 7000 ml per mole of the compound II.

### Claim 4 (depends on 1)

The process as claimed in claim 1, wherein the amount of the concentrated sulphuric used is 400 gm to 3000 gms per mole of the compound II.

### Claim 5 (depends on 1)

The process as claimed in claim 1, wherein the aqueous phase obtained after separation of the organic phase in step (d) is concentrated to obtain concentrated sulphuric acid having concentration in the range of 75% to 85% w/w.