IP Library › Granted Patent US 12,559,466
Granted Patent B2
US 12,559,466 · App. 16/977,638 · Granted Feb 24, 2026

Process for preparation of intermediates

Inventors: Santosh Ganpat Shelke (Mumbai, IN); Talati Paresh Vithaldas (Mumbai, IN); Jaidev Rajnikant Shroff (Dubai, AE); Vikram Rajnikant Shroff (Dubai, AE)
Assignee: UPL LTD
C07D301/28A01N25/12A01N43/653C07C29/143C07D249/12
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,559,466
App. No.
16/977,638
Granted
Feb 24, 2026
Kind
B2
Abstract

Disclosed herein is a process for preparation of 1-chloro-2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)propan-2-ol (compound of formula (I)) and 2-(1-chlorocyclopropyl)-2-[(2-chlorophenyl)methyl]oxirane (compound of formula (II)), which are synthetic intermediates in the preparation of triazole fungicides. The process comprises reacting a Grignard reagent of 2-chlorobenzyl halide with 1-chloro-1-chloroacetylcyclopropane, wherein said reaction is carried out at temperatures between 0° C. and 100° C. and characterized in that said reaction is carried out in a solvent system comprising methyl tetrahydrofuran and toluene.

Claims (17)

1 . A process for preparation of a mixture of 1-chloro-2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)propan-2-ol of formula (I)

and 2-(1-chlorocyclopropyl)-2-[(2-chlorophenyl)methyl]oxirane of formula (II)

comprising reacting a Grignard reagent of 2-chlorobenzyl halide with 1-chloro-1-chloroacetylcyclopropane,

wherein said reaction is carried out at temperatures between 0° C. and 40° C. and

characterized in that said reaction is carried out in a solvent system comprising methyl tetrahydrofuran and toluene in a volume ratio of methyl tetrahydrofuran to toluene of 1:1.5 to 1:5, and

further characterized that said mixture comprises 1-chloro-2-[2-(2-chlorophenyl)ethyl]benzene in an amount of 3 to 5% by weight.

2 . A process for preparing prothioconazole comprising:

(a) reacting a Grignard reagent of 2-chlorobenzyl halide with 1-chloro-1-chloroacetylcyclopropane in a solvent system comprising methyl tetrahydrofuran and toluene in a volume ratio of methyl tetrahydrofuran to toluene of 1:1.5 to 1:5 to form a mixture of 1-chloro-2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)propan-2-ol and 2-(1-chlorocyclopropyl)-2-[(2-chlorophenyl)methyl]oxirane,

wherein said reaction is carried out at temperatures between 0° C. and 40° C., and

said mixture comprises 1-chloro-2-[2-(2-chlorophenyl)ethyl]benzene in an amount of 3 to 5% by weight; and

preparing prothioconazole from the product of step (a).

3 . A process for preparing prothioconazole comprising:

(a) reacting a Grignard reagent of 2-chlorobenzyl halide with 1-chloro-1-chloroacetylcyclopropane in a solvent system comprising methyl tetrahydrofuran and toluene in a volume ratio of methyl tetrahydrofuran to toluene of 1:1.5 to 1:5 to form a mixture of 1-chloro-2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)propan-2-ol and 2-(1-chlorocyclopropyl)-2-[(2-chlorophenyl)methyl]oxirane,

wherein said reaction is carried out at temperatures between 0° C. and 40° C., and

said mixture comprises 1-chloro-2-[2-(2-chlorophenyl)ethyl]benzene in an amount of 3 to 5% by weight;

(b) reacting the step (a) product with 1,2,4-triazole to produce 2-(1-chlorocyclopropyl)-1-(2-chlorophenyl)-3-(1H-1,2,4-triazol-1-yl) propan-2-ol; and

(c) reacting step (b) product with sulfur to produce prothioconazole.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 9, 2021
From: SHELKE, SANTOSH GANPAT; VITHALDAS, TALATI PARESH; SHROFF, JAIDEV RAJNIKANT; SHROFF, VIKRAM RAJNIKANT
To: UPL LTD
Reel/Frame 058342/0708 →
Priority Claims (1)
IN 201831008255 · Mar 6, 2018 · national
Continuity (1)
Related Publication 20200399236A1 · Dec 24, 2020
References Cited (12)
US 4913727A · Stroech · 1990 [cited by examiner]
US 5099040A · Rosen · 1992 [cited by examiner]
CN 106749057A · 2017 [cited by applicant]
CN 107628928A · 2018 [cited by applicant]
DE 3942240A1 · 1991 [cited by applicant]
DE 4030039A1 · 1992 [cited by applicant]
CN 107628928—machine English translation -original document publication date is Jan. 26, 2018. [cited by examiner]
Wang (Synthesis of Prothioconazole, Nongyao, 48(3), 172-173, 201; 2009). [cited by examiner]
Arnett (J. Am. Chem. Soc., 1965, 87 (7), pp. 1541-1553). [cited by examiner]
Parin D Shah (International Journal of Advance Research in Science and Engineering IJARSE, vol. No. 3, Special Issue (01), Sep. 2014). [cited by examiner]
Monticelli et al. (Monatsh Chem (2017) 148:37-48). [cited by examiner]
International Search Report and Written Opinion for International Application PCT/IB2018/053974; International Filing Date: Jun. 4, 2018; Date of Mailing: Sep. 4, 2018; 11 pages. [cited by applicant]