首页> 外国专利> PROCESS FOR PREPARING DIAZONAPHTHOQUINONESULFONYL CHLORIDE USING DIPHOSGENE AND TRIPHOSGENE

PROCESS FOR PREPARING DIAZONAPHTHOQUINONESULFONYL CHLORIDE USING DIPHOSGENE AND TRIPHOSGENE

机译:用二茂铁和三茂铁制备二氮杂萘并异磺酰氯的方法

摘要

PROBLEM TO BE SOLVED: To provide a safe process for preparing a diazonaphthoquinonesulfonyl chloride which is a useful intermediate in electronic and dyestuff industries.;SOLUTION: The process for preparing the diazonaphthoquinonesulfonyl chloride represented by formulae 1 to 3 using diphosgene or triphosgene is carried out as follows. Sodium diazonaphthoquinonesulfonate is reacted with an organic base in a molar ratio within the range of (1:1.5) to (1:2.5) in the presence of the diphosgene or triphosgene in a molar ratio of the sodium diazonaphthoquinonesulfonate/diphosgene or triphosgene within the range of (1:1) to (1:1.5) in an organic solvent at a temperature within the range of -50 to 5°C for a period within the range of 40-90 min and the temperature is subsequently increased to 20-25°C. The solvent and base are then removed from the relational mixture under a vacuum to provide a yellow powder product. The desired product is reprecipitated in ice water.;COPYRIGHT: (C)2004,JPO
机译:解决的问题:为了提供一种安全的方法来制备重氮萘甲醌磺酰氯,该方法在电子和染料工业中是有用的中间体。;解决方案:使用双光气或三光气制备式1至3表示的重氮萘醌磺酰氯的方法如下如下。使重氮萘醌对甲磺酸钠与有机碱在二光气或三光气存在下,以重氮萘醌磺酸钠/双光气或三光气的摩尔比在(1:1.5)至(1:2.5)的范围内反应在有机溶剂中于-50至5℃的温度范围内将(1:1)至(1:1.5)进行40-90分钟的时间,然后将温度升高至20-25 ;C。然后在真空下从相关混合物中除去溶剂和碱,得到黄色粉末产物。所需的产品在冰水中重新沉淀。;版权所有:(C)2004,日本特许厅

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