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    • 5. 发明专利
    • PRODUCTION OF L-ASPARTIC ACID
    • JPH09163993A
    • 1997-06-24
    • JP32707195
    • 1995-12-15
    • MITSUBISHI CHEM CORP
    • MORI YOSHIAKIKATO NAOKIWATANABE NAOYUKIFUJII SEIJI
    • C12P13/20C07C227/40C07C229/24C12R1/05C12R1/13
    • PROBLEM TO BE SOLVED: To efficiently obtain L-aspartic acid useful as e.g. a food additive, medicine, by converting ammonium maleate into ammonium L-aspartate with an enzyme followed by distillation to effect removal of NH3 and then acid deposition with maleic acid and neutralization of NH3 with maleic acid, and by circulating the resultant mother liquor. SOLUTION: An aqueous solution of ammonium maleate as feedstock is first subjected to isomerization reaction through enzymatic treatment with aspartase or aspartase-productive microorganisms in the presence of ammonia to yield an aqueous solution of ammonium L-aspartate. Secondly, the aqueous solution of ammonium L-aspartate is distilled to effect NH3 removal to produce monoammonium L-aspartate, whose aqueous solution is then subjected to acid deposition by use of maleic acid and/or maleic anhydride to effect deposition of L-aspartic acid crystal. Thirdly, the resultant mother liquor containing monoammonium maleate after acid deposition is used as a feedstock, an ammonia-contg. gas discharged via the column top during the distillation is absorbed into an aqueous solution prepared by use of part of the acid deposition agent, and the resultant aqueous solution is also used as a feedstock together with the mother liquor after acid deposition, thus efficiently obtaining the objective L-aspartic acid.
    • 8. 发明专利
    • ALKYL HYDANTOINS
    • JP2001064265A
    • 2001-03-13
    • JP24089299
    • 1999-08-27
    • MITSUBISHI CHEM CORP
    • TAKUMA YUUKIWATANABE NAOYUKIHARA MARI
    • C07D233/74C07D233/96
    • PROBLEM TO BE SOLVED: To obtain the subject new compound useful as an intermediate for effectively producing (L)-Boc-N-methyl-leucine and analogous compounds thereof and useful as a producing material for medical and agrochemical compounds. SOLUTION: This compound is represented by the formula (R1 is a 1-6C alkyl; R2 and R3 are each H or a 1-6C alkyl) e.g. 5-alkylidene-1-alkylhydantoin. The compound is obtained e.g. by reacting 1-substituted hydantoin with 0.8-1.5 molar times compound containing bromine (e.g. bromine or N- bromosuccinimide) in the presence of a solvent such as acetic acid at 70-120 deg.C to brominate 5-position of the hydantoin, then reacting the brominated product with 1-2 molar times phosphite based on the applied 1-substituted hydantoin and then reacting the resultant product with 1-5 molar times compound containing a carbonyl group (e.g. isobutly aldehyde) in a solvent e.g. ethanol in the presence of a base (e.g. triethylamine) at room temperature.