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US4667049A Expired / Lapsed US ⏱️ 0.0 years remaining

Method of making dialkylamino-thioxomethyl-thioalkanesulfonic acid compounds

Assignee: MC GEAN-ROHCO Inc
•
Filing: 1986-02-27
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Granted: 1987-05-19
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Expires: 2006-02-27
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Abstract

Abstract A method for the preparation of an alkali metal dialkylaminothioxomethyl-thioalkanesulfonate composition comprising reacting a monoamine with carbon disulfide to form a dithiocarbamic acid monoamine salt, reacting the salt with an alkyl sultone to form an amino thioxo methyl thioalkane sulfonate monoamine salt, and sulfonate salt with an alkali metal base to form an alkali metal salt of the amino thioxo methyl thioalkane sulfonate composition.

Inventors

  • 👤 Kurt E. Heikkila
  • 👤 Rodney K. Williams
  • 👤 Bruce A. Bohnen
  • 👤 Russell J. Pylkki

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 23:05
CPC Classifications
C; C25; C25D; C25D3/00; C25D3/02; C25D3/38

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 100 words
A method for the preparation of an improved, more pure dialkylamino-thioxomethyl-thioalkanesulfonate composition which comprises the steps of: (a) reacting a dialkyl monoamine compound with carbon disulfide in sufficient amount to form a dialkyl dithiocarbamate dialkylamine salt; (b) reacting the dialkyl dithiocarbamate dialkylamine salt with an alkyl sultone to form a dialkylamine salt of a dialkylamino-thioxomethyl-thioalkanesulfonate; and (c) reacting the dialkylamine salt of the dialkylamino-thioxomethyl-thioalkanesulfonate with an alkali metal base at a sufficient temperature (1) to form an alkali metal salt of the dialkylamino-thioxomethyl-thioalkane sulfonic acid substantially free of nonvolatile reaction by-products and impurities; and (2) to volatilize the liberated monoamine.
Claim 2
Independent Claim 100 words
A method for the preparation of an improved, more pure dialkylamino-thioxomethyl-thioalkanesulfonate composition which comprises the steps of: (a) reacting a dialkyl monoamine compound with carbon disulfide in sufficient amount to form a dialkyl dithiocarbamate dialkylamine salt; (b) reacting the dialkyl dithiocarbamate dialkylamine salt with an alkyl sultone to form a dialkylamine salt of a dialkylamino-thioxomethyl-thioalkanesulfonate; and (c) reacting the dialkylamine salt of the dialkylamino-thioxomethyl-thioalkanesulfonate with an alkali metal base at a sufficient temperature (1) to form an alkali metal salt of the dialkylamino-thioxomethyl-thioalkane sulfonic acid substantially free of nonvolatile reaction by-products and impurities; and (2) to volatilize the liberated monoamine.
Claim 3
Dependent Claim 27 words
The method of claim 1 wherein each alkyl group of the dialkyl amine is independently selected from methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, amyl or hexyl.
Claim 4
Dependent Claim 12 words
The method of claim 1 wherein the alkyl sultone comprises 1,3-propane sultone.
Claim 5
Dependent Claim 15 words
The method of claim 1 wherein the alkali metal base comprises an alkali metal hydroxide.
Claim 6
Dependent Claim 13 words
The method of claim 4 wherein the alkali metal hydroxide comprises sodium hydroxide.

References Cited (Backward Citations)

US2891065A Cited
US3023215A Cited
US3122549A Cited
US3359297A Cited
US4134803A Cited
US4272335A Cited
US4430173A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-05-18 1990-11-17 1991-05-19 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-05-18 1994-11-17 1995-05-19 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-05-18 1998-11-17 1999-05-19 $7700.00 Window Closed / Lapsed

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