Isothiuronium salt and method of manufacturing the same and method for manufacturing substituted benzene ethyl mercaptan compounds
A technology of phenylethane mercaptan and compound, applied in the field of organic synthesis, can solve the problems of complicated operation, low yield, high environmental pressure and the like, and achieves the effects of easy industrialization, simple operation and high yield
Active Publication Date: 2011-01-19
ZHEJIANG APELOA JIAYUAN PHARMA +1
View PDF1 Cites 0 Cited by
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Patent US2402613 discloses a method for preparing mercaptans by catalytic hydrogenation and hydrolysis of thiocarbonyl groups. This method has high cost, low yield, cumbersome operation, and cannot realize industrial production
Patent US4161493 reports the exchange reaction of thioaldehyde or thioketone and thiol to obtain corresponding products. Although this method has the characteristics of high selectivity and conversion rate, it is difficult to separate the main product and by-product, thus hindering the industrial application of this method.
The article ("Journal of Chemical Society of Japan", 1987, (7), P.1502-1504) published by Murai Shinji etc. adopts the method that sulfur, carbon monoxide and water react with aromatic hydrocarbon ketone and aldehyde to prepare mercaptan, although the method has higher yield High, but the carbon monoxide discharged after the reaction has a great pressure on environmental protection, which limits the commercial production of this method
Method used
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View moreImage
Smart Image Click on the blue labels to locate them in the text.
Smart ImageViewing Examples
Examples
Experimental program
Comparison scheme
Effect test
Embodiment 1
Embodiment 2
Embodiment 3
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More PUM
Login to View More Abstract
The invention belongs to the organic synthesis field, in particular to the isothiourca salt and the preparation method and the method using the isothiourca salt to prepare and replace the 2-phenylethylmercaptan component. The structural formula of the isothiourca salt (IV) refers to the drawing, wherein, R is the alkyl of the hydrogen, halogen atom or C1-C4 and X is the anionic group which can acidify. The invention also discloses the preparation method of the isothiourca salt and the method using the isothiourca to prepare and replace the 2-phenylethylmercaptan component. Because of adoptingthe above technical proposal, the invention provides the isothiourca salt to replace the 2-phenylethylmercaptan component. Using the method to prepare and replace the 2-phenylethylmercaptan componentis characterized by simple operation, low cost, high yield and easy industrialization.
Description
technical field The invention belongs to the field of organic synthesis, and in particular relates to isothiouronium salts, a preparation method thereof and a method for preparing substituted phenethanethiol compounds with it. Background technique Substituted phenylethanethiol compounds are important intermediates in organic synthesis, and are also raw materials for the preparation of phenylethanesulfonic acid, a good resolution agent for amino acids such as leucine. Patent US2402613 discloses a method for preparing mercaptans by catalytic hydrogenation and hydrolysis of thiocarbonyl groups. This method has high cost, low yield, cumbersome operation, and cannot realize industrial production. Patent US4161493 reports the exchange reaction of thioaldehyde or thioketone and thiol to obtain corresponding products. Although this method has the characteristics of high selectivity and conversion rate, it is difficult to separate the main product and by-product, thus hindering the i...
Claims
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More Application Information
Patent Timeline
Login to View More Patent Type & Authority Patents(China)
IPC IPC(8): C07C335/30C07C319/02C07C321/10
Inventor 谭龙泉申屠阳靳小舜陈攀峰金毅强丁永菊
Owner ZHEJIANG APELOA JIAYUAN PHARMA



