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Manufacturing method null of S hydroxypropyl L

机译:S羟丙基L的制造方法无效

摘要

PURPOSE: To profitably obtain the subject cysteine compound by reacting cysteine hydrochloride with allylalcohol in the presence of a radical initiator. ;CONSTITUTION: (A) Cysteine or cysteine hydrochloride is reacted with (B) allylalcohol in the presence of (C) a radical initiator (e.g. sodium persulfate) and (D) a reducing agent (e.g. ferrous chloride) under the irradiation of light (e.g. light having a wave length of 250-260nm for approximately 10-60min) to obtain the objective cysteine compound. The component A and the component B are used in a molar ratio of approximately 1:1.5-2.5, and the component C and the component D are used in amounts of 10wt.% and 5-10wt.%, respectively. The solvent is e.g. water or alcohol. The reaction is preferably performed at 0°C to room temperature for 5-60min. Further, 2,2-dimethylthiazolidine-4- carboxylic acid is preferably reacted with a 3-halogen-1-propanol at a pH of 8-10, and the obtained reaction mixture is reacted with a reducing agent (e.g. sodium sulfide).;COPYRIGHT: (C)1996,JPO
机译:目的:通过在自由基引发剂的存在下使半胱氨酸盐酸盐与烯丙醇反应,以有利地获得目标半胱氨酸化合物。 ;组成:(A)在(C)自由基引发剂(例如过硫酸钠)和(D)还原剂(例如氯化亚铁)的存在下,(C)半胱氨酸或半胱氨酸盐酸盐与(B)烯丙醇反应(例如波长为250-260nm的光持续约10-60min)以获得目标半胱氨酸化合物。组分A和组分B的摩尔比约为1:1.5-2.5,组分C和组分D的用量分别为10wt。%和5-10wt。%。溶剂是例如水或酒精。该反应优选在0℃至室温下进行5-60分钟。此外,优选使2,2-二甲基噻唑烷-4-羧酸与3-卤素-1-丙醇在pH 8-10下反应,并且将所得反应混合物与还原剂(例如硫化钠)反应。版权所有:(C)1996,日本特许厅

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