IP Library Granted Patent US 9,365,471
Granted Patent B2
US 9,365,471 · App. 14/213,494 · Granted Jun 14, 2016

Substituted phenylsulfur trifluoride and other like fluorinating agents

Inventor: Teruo Umemoto (Westminster, CO)
Assignee: UBE INDUSTRIES, LTD.
C07C17/18C07B39/00C07C17/093C07C17/16C07C17/361C07C45/65C07C51/60C07C319/14C07C319/20C07C323/19C07C381/00C07C2101/14
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Quick Facts
Patent No.
US 9,365,471
App. No.
14/213,494
Granted
Jun 14, 2016
Kind
B2
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. Finally, various intermediate compounds for use in preparing substituted phenylsulfur trifluorides are provided.

Claims (34)

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

contacting a fluorinating agent of formula (I):

in which

R 1a and R 1b are independently a hydrogen atom; a primary or secondary alkyl group having from one to eight carbon atoms; or a primary, secondary, or tertiary alkyl group having two to eight carbon atoms and at least one ether linkage; and

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

R 3 is a hydrogen atom; a primary, secondary, or tertiary alkyl group having from one to eight carbon atoms; or a primary, secondary, or tertiary alkyl group having two to eight carbon atoms and at least one ether linkage; and

wherein, when R 3 is a hydrogen atom, at least two of R 1a , R 1b , R 2a and R 2b each is independently a halogen atom; a primary, secondary, or tertiary alkyl group having from one to eight carbon atoms wherein R 1a and R 1b are not a halogen atom or a tertiary alkyl group; or a primary, secondary, or tertiary alkyl group having two to eight carbon atoms and at least one ether linkage; or, at least one of R 1a , R 1b , R 2a , and R 2b is a primary, secondary, or tertiary alkyl group having two to eight carbon atoms and at least one ether linkage; and

wherein, when R 3 is a primary alkyl group having one to eight carbon atoms, at least one of R 1a , R 1b , R 2a , and R 2b is a halogen atom; a primary, secondary, or tertiary alkyl group having from one to eight carbon atoms wherein R 1a and R 1b are not a halogen atom or a tertiary alkyl group; or a primary, secondary, or tertiary alkyl group having two to eight carbon atoms and at least one ether linkage; 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;

with the target compound under conditions that allow one or more fluorine atoms to be introduced into the target compound.

2. The method of claim 1 , 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.

3. The method of claim 1 , wherein the target compound has one or more sulfur or sulfur-containing groups which are replaced by the introduction of the one or more fluorine atoms.

4. The method of claim 1 , wherein the fluorinating agent is selected from the group consisting of 2,6-dimethyl-4-tert-butylphenylsulfur trifluoride; 2,6-dimethyl-3-chloro-4-tert-butylphenylsulfur trifluoride; 2,6-dimethyl-3,5-dichloro-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; 2,4,6-tri(isopropyl)phenylsulfur trifluoride; 2,6-bis(methoxymethyl)phenylsulfur trifluoride; 2,6-bis(methoxymethyl)-4-tert-butylphenylsulfur trifluoride; 2,6-bis(ethoxymethyl)-4-tert-butylphenylsulfur trifluoride; 2,6-bis(isopropoxymethyl)-4-tert-butylphenylsulfur trifluoride; 2,6-bis(isobutoxymethyl)-4-tert-butylphenylsulfur trifluoride; and 2,6-bis(tert-butoxymethyl)-4-tert-butylphenylsulfur trifluoride.

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

contacting a fluorinating agent of formula (Ia):

in which:

R 1a and R 1b are independently a hydrogen atom; a primary or secondary alkyl group having from one to eight carbon atoms; or a primary, secondary, or tertiary alkyl group having two to eight carbon atoms and at least one ether linkage;

R 2a′ and R 2b′ are independently a hydrogen atom or a halogen atom; and

R 3 is a hydrogen atom; a primary, secondary, or tertiary alkyl group having from one to eight carbon atoms; or a primary, secondary, or tertiary alkyl group having two to eight carbon atoms and at least one ether linkage;

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 or at least one of R 1a and R 1b is a primary, secondary, or tertiary alkyl group having two to eight carbon atoms and at least one ether linkage, 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 or a primary, secondary, or tertiary alkyl group having two to eight carbon atoms and at least one ether linkage;

with the target compound under conditions that allow one or more fluorine atoms to be introduced into the target compound.

6. The method of claim 5 , 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.

7. The method of claim 5 , wherein the target compound has one or more sulfur or sulfur-containing groups which are replaced by the introduction of the one or more fluorine atoms.

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

contacting a fluorinating agent of 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, 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;

with the target compound under conditions that allow one or more fluorine atoms to be introduced into the target compound.

9. The method of claim 8 , 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.

10. The method of claim 8 , wherein the target compound has one or more sulfur or sulfur-containing groups which are replaced by the introduction of the one or more fluorine atoms.

Assignments (4)
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 May 12, 2014
From: UMEMOTO, TERUO
To: IM&T RESEARCH, INC.
Reel/Frame 032869/0129 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2014
From: IM&T RESEARCH, INC.
To: UBE INDUSTRIES, LTD.
Reel/Frame 032869/0170 →
Continuity (6)
Division 12886286 · Sep 20, 2010
Continuation 12367171 · Feb 6, 2009
Continuation 12106460 · Apr 21, 2008
Division 11828162 · Jul 25, 2007
Continuation In Part 11494983 · Jul 28, 2006
Related Publication 20140235898A1 · Aug 21, 2014