IP Library Granted Patent US 8,933,260
Granted Patent B2
US 8,933,260 · App. 14/049,820 · Granted Jan 13, 2015

Process for preparing alkoxycarbonyl isothiocyanate

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 8,933,260
App. No.
14/049,820
Granted
Jan 13, 2015
Kind
B2
Abstract

Provided herein are processes for the preparation of alkoxycarbonyl isothiocyanates from alkyl chloroformates and thiocyanates in toluene by controlling the amounts of water and catalyst.

Claims (22)

1. A process for the preparation of an alkoxycarbonyl isothiocyanate of the formula

wherein R represents C 1 -C 4 alkyl

which comprises contacting a salt of thiocyanate ( − SCN) with an alkyl chloroformate in toluene solvent in the presence of a) from about 0.01 to about 1.00 molar equivalents of water and b) from about 0.01 to about 1.00 molar equivalents of a catalyst comprising a six-membered mononuclear or ten-membered fused polynuclear aromatic, heterocyclic compound having 1 or 2 nitrogen atoms as the only heteroatoms in the ring, at a temperature from about 0° C. to about 110° C., wherein the alkyl chloroformate has the following formula:

2. The process of claim 1 , wherein R is methyl or ethyl.

3. The process of claim 2 , wherein R is ethyl.

4. The process of claim 1 , wherein the salt of thiocyanate is a sodium, potassium or ammonium salt.

5. The process of claim 4 , wherein the salt of thiocyanate is a sodium salt.

6. The process of claim 1 , wherein the catalyst is pyridine, quinoline, pyrimidine, pyrazine, or quinoxaline optionally substituted with one or more alkyl, halo, or alkoxy groups, wherein the pyridine, quinoline, pyrimidine, pyrazine, or quinoxaline is unsubstituted at the 2-position.

7. The process of claim 6 , wherein the catalyst is pyridine.

8. The process of claim 1 , wherein about 0.05 to about 0.1 molar equivalents of water are employed.

9. The process of claim 8 , wherein about 0.1 molar equivalents of water are employed.

10. The process of claim 1 , wherein about 0.01 to about 0.03 molar equivalents of catalyst are employed.

11. The process of claim 10 , wherein about 0.01 equivalents of catalyst are employed.

12. The process of claim 1 , wherein the temperature is from about 20° C. to about 40° C.

13. The process of claim 12 , wherein the temperature is about 30° C.

14. The process of claim 1 , wherein

a. R is methyl or ethyl;

b. the salt of thiocyanate is a sodium, potassium or ammonium salt;

c. the catalyst is pyridine, quinoline, pyrimidine, pyrazine, or quinoxaline optionally substituted with one or more alkyl, halo, or alkoxy groups, wherein the pyridine, quinoline, pyrimidine, pyrazine, or quinoxaline is unsubstituted at the 2-position;

d. about 0.05 to about 0.1 molar equivalents of water are employed;

e. about 0.01 to about 0.03 molar equivalents of catalyst are employed; and

f. wherein the temperature is from about 20° C. to about 40° C.

Assignments (2)
CHANGE OF NAME Recorded Nov 8, 2021
From: DOW AGROSCIENCES LLC
To: CORTEVA AGRISCIENCE LLC
Reel/Frame 058044/0184 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 19, 2014
From: FISK, JASON S; BLAND, DOUGLAS C; FRYCEK, GEORGE J
To: DOW AGROSCIENCES LLC
Reel/Frame 032246/0077 →