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    • 1. 发明专利
    • AT444284T
    • 2009-10-15
    • AT03012670
    • 2003-06-04
    • SALTIGO GMBH
    • BOSCH BORIS ELMARGERHARTZ FRANK
    • C07C303/38B01J31/22C07B53/00C07C29/143C07C311/09C07C311/18C07C319/12C07C323/62
    • Production of mono-N-sulfonylated diamine compounds comprises reaction of a diamine compound with a sulfonyl halide in the presence of water, organic solvent and a base. Production of mono-N-sulfonylated diamine compounds (I) of formula (1) comprises reaction of a diamine compound of formula (2) with a sulfonyl halide of formula (3) in the presence of water, organic solvent and a base. R3SO2X (3) R1 and R2 = 1-20C alkyl, 4-15C aryl, 5-16C arylalkyl or R1 and R2 together form a 3-12C alkylene; R3 = 1-20C alkyl, optionally fluorinated or 4-15C aryl; and X = F, Cl, Br or I. Independent claims are also included for the following: (1) solutions (II) containing the mono-N-sulfonylated diamine compounds (I) prepared by the process followed by at least partial removal of water; and (2) catalysts (III) prepared from the solutions (II) by reaction with organometallic compounds of formula (4). (MXn(R4))2 (4) M = Ru, Rh or Ir; R4 = 6-12C aryl, optionally substituted by 1-8C alkyl, benzyl or phenyl, or cyclopentadienyl optionally substituted by up to 5 groups or indenyl; and n = 1 or 2.
    • 5. 发明专利
    • DE50311954D1
    • 2009-11-12
    • DE50311954
    • 2003-06-04
    • SALTIGO GMBH
    • BOSCH BORIS ELMAR DRGERHARTZ FRANK
    • C07C303/38B01J31/22C07B53/00C07C29/143C07C311/09C07C311/18C07C319/12C07C323/62
    • Production of mono-N-sulfonylated diamine compounds comprises reaction of a diamine compound with a sulfonyl halide in the presence of water, organic solvent and a base. Production of mono-N-sulfonylated diamine compounds (I) of formula (1) comprises reaction of a diamine compound of formula (2) with a sulfonyl halide of formula (3) in the presence of water, organic solvent and a base. R3SO2X (3) R1 and R2 = 1-20C alkyl, 4-15C aryl, 5-16C arylalkyl or R1 and R2 together form a 3-12C alkylene; R3 = 1-20C alkyl, optionally fluorinated or 4-15C aryl; and X = F, Cl, Br or I. Independent claims are also included for the following: (1) solutions (II) containing the mono-N-sulfonylated diamine compounds (I) prepared by the process followed by at least partial removal of water; and (2) catalysts (III) prepared from the solutions (II) by reaction with organometallic compounds of formula (4). (MXn(R4))2 (4) M = Ru, Rh or Ir; R4 = 6-12C aryl, optionally substituted by 1-8C alkyl, benzyl or phenyl, or cyclopentadienyl optionally substituted by up to 5 groups or indenyl; and n = 1 or 2.