IP Library Granted Patent US 7,265,247
Granted Patent B1
US 7,265,247 · App. 11/494,983 · Granted Sep 4, 2007

Substituted phenylsulfur trifluoride and other like fluorinating agents

Assignee: IM&T Research, Inc.
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Quick Facts
Patent No.
US 7,265,247
App. No.
11/494,983
Granted
Sep 4, 2007
Kind
B1
Abstract

Novel substituted phenylsulfur trifluorides that act as fluorinating agents are disclosed. Also disclosed are methods for their preparation and methods for their use in introducing one or more fluorine atoms into target substrate compounds.

Claims (27)

1. A compound of the formula (I):

in which

R 1a and R 1b are independently a hydrogen atom or a primary or secondary alkyl group having from one to eight carbon atoms;

R 2a and R 2b are independently a hydrogen atom or a primary, secondary, or tertiary alkyl group having from one to eight carbon atoms; and

R 3 is a hydrogen atom, a halogen atom, or a primary, secondary, or tertiary alkyl group having from one to eight carbon atoms;

wherein, when R 3 is a hydrogen atom, at least two of R 1a , R 1b , R 2a , and R 2b are primary, secondary, or tertiary alkyl groups having from one to eight carbon atoms and the others are a hydrogen atom, and wherein, when R 3 is a primary alkyl group having from one to eight carbon atoms, at least one of R 1a , R 1b , R 2a , and R 2b is a primary, secondary, or tertiary alkyl group having from one to eight carbon atoms and the others are a hydrogen atom, and wherein when at least two of R 2a , R 2b , and R 3 are tertiary alkyl groups, the tertiary alkyl groups are non-adjacent.

2. The compound of claim 1 , wherein the primary, secondary, or tertiary alkyl groups have from one to four carbon atoms.

3. The compound of claim 1 , wherein R 3 is a tertiary alkyl group.

4. The compound of claim 3 , wherein the tertiary group is tert-butyl group.

5. The compound of claim 1 , wherein the compound is selected from the group consisting of 2,6-dimethyl-4-tert-butylphenylsulfur trifluoride; 4-tert-butylphenylsulfur trifluoride; 2,4,6-trimethylphenylsulfur trifluoride; 2,4-dimethylphenylsulfur trifluoride; 2,5-dimethylphenylsulfur trifluoride; 2,6-dimethylphenylsulfur trifluoride; 4-fluorophenylsulfur trifluoride; 4-chlorophenylsulfur trifluoride; 3-methyl-4-chlorophenylsulfur trifluoride; and 2,4,6-tri(isopropyl)phenylsulfur trifluoride.

6. The compound of claim 1 , wherein the compound is 2,6-dimethyl-4-tert-butylphenylsulfur trifluoride.

7. A compound according to claim 1 , wherein the compound is a compound of the formula (II):

in which:

R 1a and R 1b are independently a hydrogen atom or a primary or secondary alkyl group having from one to eight carbon atoms; and

R 3 is a hydrogen atom, a halogen atom, or a primary, secondary, or tertiary alkyl group having from one to eight carbon atoms;

wherein when R 3 is a hydrogen atom, R 1a and R 1b are independently a primary or secondary alkyl group having from one to eight carbon atoms, and wherein, when R 3 is a primary alkyl group having one to eight carbon atoms, at least one of R 1a and R 1b is a primary or secondary alkyl group having from one to eight carbon atoms and the other is a hydrogen atom.

8. The compound of claim 7 , wherein the primary, secondary, or tertiary alkyl groups have from one to four carbon atoms.

9. The compound of claim 7 , wherein R 3 is a tertiary alkyl group.

10. The compound of claim 9 , wherein the tertiary group is tert-butyl group.

11. A method of introducing one or more fluorine atoms into a target compound comprising:

contacting a fluorinating agent of formula (I) from claim 1 with the target compound under conditions that allow one or more fluorine atoms to be introduced into the target compound.

12. The method of claim 11 , wherein the target compound has one or more oxygen or oxygen-containing groups which are replaced by the introduction of the one or more fluorine atoms.

13. The method of claim 11 , wherein the fluorinating agent is selected from the group consisting of 2,6-dimethyl-4-tert-butylphenylsulfur trifluoride; 4-tert-butylphenylsulfur trifluoride; 2,4,6-trimethylphenylsulfur trifluoride; 2,4-dimethylphenylsulfur trifluoride; 2,5-dimethylphenylsulfur trifluoride; 2,6-dimethylphenylsulfur trifluoride; 4-fluorophenylsulfur trifluoride; 4-chlorophenylsulfur trifluoride; 3-methyl-4-chlorophenylsulfur trifluoride; and 2,4,6-tri(isopropyl)phenylsulfur trifluoride.

14. The method of claim 11 , wherein the fluorinating agent is 2,6-dimethyl-4-tert-butylphenylsulfur trifluoride.

15. A method of introducing one or more fluorine atoms into a target compound comprising:

contacting a fluorinating agent of formula (II) from claim 7 with the target compound under conditions that allow one or more fluorine atoms to be introduced into the target compound.

16. The method of claim 15 , wherein the target compound has one or more oxygen or oxygen-containing groups which are replaced by the introduction of the one or more fluorine atoms.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 1, 2024
From: UBE CORPORATION
To: INNER MONGOLIA YONGTAI CHEMICAL CO., LTD.
Reel/Frame 068146/0767 →
CHANGE OF NAME & ADDRESS Recorded Jul 14, 2023
From: UBE INDUSTRIES, LTD.
To: UBE CORPORATION
Reel/Frame 064274/0902 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2011
From: IM&T RESEARCH, INC.
To: UBE INDUSTRIES, LTD.
Reel/Frame 025751/0119 →