Abstract: The present invention provides an industrially advantageous method for producing bis(halosulfonyl)amine that makes it possible to inhibit the rapid generation of gas and reduce the amount of halogenating agent used by controlling the reaction rate among sulfamic acid, the halogenating agent and a halosulfonic acid to nearly a constant rate from the initial stage to the final stage of the reaction. The method for producing bis(halosulfonyl)amine of the present invention allows the obtaining of a bis(halosulfonyl)amine such as N-(fluorosulfonyl)-N-(chlorosulfonyl)amine or bis(chlorosulfonyl)amine by a production method that includes heating a mixture containing sulfamic acid and a halosulfonic acid to a temperature higher than room temperature, adding a halogenating agent thereto, and allowing to react while adjusting to a prescribed temperature.

Abstract: A compound [I] such as ammonium N-(chlorosulfonyl)-N-(fluorosulfonyl)imide is reacted with hydrogen fluoride to obtain a compound [II] such as ammonium N,N-di(fluorosulfonyl)imide. The obtained compound [II] is reacted with an alkali metal compound or the like to obtain a compound [IV] such as an N,N-di(fluorosulfonyl)imide alkali metal salt.

Abstract: By reacting a fluorine-containing sulfonylimide ammonium salt such as ammonium N,N-di(fluorosulfonyl)imide with an alkali metal hydroxide such as lithium hydroxide, potassium hydroxide or sodium hydroxide under reduced pressure and at a low temperature of approximately 40° C., a fluorine-containing sulfonylimide alkali metal salt such as lithium N,N-di(fluorosulfonyl)imide, potassium N,N-di(fluorosulfonyl)imide or sodium N,N-di(fluorosulfonyl)imide is obtained.

Abstract: A compound [II] such as ammonium N,N-di(fluorosulfonyl)imide is obtained by reacting a compound [I] such as N,N-di(chlorosulfonyl)imide and NH4F (HF)p. A compound [IV] such as an N,N-di(fluorosulfonyl)imide alkali metal salt is obtained by reacting the obtained compound [II] and an alkali metal compound or the like.

Abstract: The present invention provides an industrially advantageous method for producing bis(halosulfonyl)amine that makes it possible to inhibit the rapid generation of gas and reduce the amount of halogenating agent used by controlling the reaction rate among sulfamic acid, the halogenating agent and a halosulfonic acid to nearly a constant rate from the initial stage to the final stage of the reaction. The method for producing bis(halosulfonyl)amine of the present invention allows the obtaining of a bis(halosulfonyl)amine such as N-(fluorosulfonyl)-N-(chlorosulfonyl)amine or bis(chlorosulfonyl)amine by a production method that includes heating a mixture containing sulfamic acid and a halosulfonic acid to a temperature higher than room temperature, adding a halogenating agent thereto, and allowing to react while adjusting to a prescribed temperature.

Abstract: A compound [II] such as ammonium N,N-di(fluorosulfonyl)imide is obtained by reacting a compound [I] such as N,N-di(chlorosulfonyl)imide and NH4F (HF)p. A compound [IV] such as an N,N-di(fluorosulfonyl)imide alkali metal salt is obtained by reacting the obtained compound [II] and an alkali metal compound or the like.

Abstract: By reacting a fluorine-containing sulfonylimide ammonium salt such as ammonium N,N-di(fluorosulfonyl)imide with an alkali metal hydroxide such as lithium hydroxide, potassium hydroxide or sodium hydroxide under reduced pressure and at a low temperature of approximately 40° C., a fluorine-containing sulfonylimide alkali metal salt such as lithium N,N-di(fluorosulfonyl)imide, potassium N,N-di(fluorosulfonyl)imide or sodium N,N-di(fluorosulfonyl)imide is obtained.

Abstract: A compound [I] such as ammonium N-(chlorosulfonyl)-N-(fluorosulfonyl)imide is reacted with hydrogen fluoride to obtain a compound [II] such as ammonium N,N-di(fluorosulfonyl)imide. The obtained compound [II] is reacted with an alkali metal compound or the like to obtain a compound [IV] such as an N,N-di(fluorosulfonyl)imide alkali metal salt.

Abstract: A process is provided capable of producing 3-methylthiopropanal with subgeneration of high-boiling impurities being favorably inhibited. The process for producing 3-methylthiopropanal, includes reacting acrolein with methylmercaptan in the presence of a triallylamine compound represented by the formula (I): wherein each of R1 to R3 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. The reaction of acrolein with methylmercaptan is preferably performed further in the presence of an organic acid. The triallylamine compound represented by the formula (I) is preferably used in an amount of from 0.01 to 1.0 mol based on one mole of the organic acid and in an amount of from 0.1 to 2.0 mmoles based on one mole of methylmercaptan.

Abstract: A process is provided capable of producing 3-methylthiopropanal with subgeneration of high-boiling impurities being favorably inhibited. The process for producing 3-methylthiopropanal, includes reacting acrolein with methylmercaptan in the presence of a triallylamine compound represented by the formula (I): wherein each of R1 to R3 represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. The reaction of acrolein with methylmercaptan is preferably performed further in the presence of an organic acid. The triallylamine compound represented by the formula (I) is preferably used in an amount of from 0.01 to 1.0 mol based on one mole of the organic acid and in an amount of from 0.1 to 2.0 mmoles based on one mole of methylmercaptan.