IP Library Granted Patent US 8,716,513
Granted Patent B2
US 8,716,513 · App. 13/387,887 · Granted May 6, 2014

Process for production of bis-quaternary ammonium salt, and novel intermediate

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Quick Facts
Patent No.
US 8,716,513
App. No.
13/387,887
Granted
May 6, 2014
Kind
B2
Abstract

Object To provide a method for producing a bis-quaternary ammonium salt efficiently and a novel synthetic intermediate thereof. Solution The present invention relates to a method for producing a bis-quaternary ammonium salt represented by a general formula [3] which comprises reacting a disulfonic acid ester represented by a general formula [1] (in the formula, definitions of two R 1 's and T are as described in claim 1 ) with a tertiary amine represented by a general formula [2] (in the formula, definitions of R 3 to R 5 are as described in claim 1 ), and a disulfonic acid ester represented by a general formula [1′] (in the formula, two R 16 's represent independently a halogen atom or a C1-C3 fluoroalkyl group, and two m's represent independently an integer of 1 to 5).

Claims (9)

1. A method for producing a bis-quaternary ammonium salt represented by a formula (3), which comprises reacting a disulfonic acid ester represented by a formula (1) with a tertiary amine represented by a formula (2):

wherein R 1 represents an alkyl group, which may have at least one substituent, a haloalkyl group, a heteroatom-containing alkyl group, which may have at least one substituent, a phenyl group, which may have at least one substituent selected from the group consisting of halogen and a C 1 -C 3 fluoroalkyl group independently, an aralkyl group, which may have at least one substituent, a heterocyclic group, which may have at least one substituent, or an unsaturated hydrocarbon group, and T represents a C 1 -C 3 alkylene chain,

wherein R 3 to R 5 represent independently an alkyl group or a heteroatom-containing alkyl group, R 3 and R 4 or R 3 to R 5 and nitrogen bonding thereto may form a heterocycle, and

wherein R 1 , R 3 to R 5 , and T are the same as the above.

2. The producing method according to claim 1 , wherein T is a methylene group.

3. The producing method according to claim 1 , wherein the tertiary amine represented by the formula (2) is pyridine, 3-methylpyridine, 3,5-dimethylpyridine, 1-methylimidazole, 1,2-dimethylimidazole, or tributylamine.

4. A disulfonic acid ester represented by a following formula (1′):

wherein, two R 16 s represent independently halogen or a C 1 -C 3 fluoroalkyl group, and two ms represent independently an integer from 1 to 5.

5. The producing method according to claim 1 , wherein R 1 is a methyl group or trifluoromethyl group.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 24, 2018
From: WAKO PURE CHEMICAL INDUSTRIES, LTD.
To: FUJIFILM WAKO PURE CHEMICAL CORPORATION
Reel/Frame 046697/0291 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2012
From: OKAMOTO, KUNIAKI; WATAHIKI, TSUTOMU; SUMINO, MOTOSHIGE
To: WAKO PURE CHEMICAL INDUSTRIES, LTD.
Reel/Frame 027622/0415 →