Synthetic method of tetrabromo neopentane

A technology for the synthesis of bromopentane, which is applied in the fields of chemical instruments and methods, preparation of halogenated hydrocarbons, preparation of sulfonate, etc., can solve problems such as easy moisture absorption and complicated feeding process, so as to reduce usage and environment Contamination, effects of mild reaction conditions

Pending Publication Date: 2020-07-10
CHONGQING MEDICAL & PHARMA COLLEGE
View PDF2 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The second method uses pentaerythritol as a raw material, first reacts with p-toluenesulfonyl chloride to activate the hydroxyl group, and then replaces it with sodium bromide. Because one molecule of pentaerythritol needs four equivalents of p-toluenesulfonyl chloride, p-toluenesulfonyl chloride is Solid state, easy to absorb moisture, resulting in more complicated feeding process in production

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 more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Synthetic method of tetrabromo neopentane
  • Synthetic method of tetrabromo neopentane
  • Synthetic method of tetrabromo neopentane

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] Add 1.3kg (9.6mol) of pentaerythritol and 6.5L of pyridine into a 20L three-necked flask, and add 5.5L (42mol) of benzenesulfonyl chloride dropwise under stirring. Control the rate of addition so that the reaction temperature is controlled below 35°C, and the drop is completed within 2 hours. After the dropwise addition, continue to stir the reaction at 40°C for 3h until the reaction is complete. After the reaction was completed, the cold bath was cooled to 0°C, and then the above reaction system was added dropwise to 5L of ice water for crystallization. During the dropping process, the temperature was controlled to be lower than 40°C, and a white granular precipitate was formed. After filtering, the filter cake was washed twice with water (5 L×2), once with 5% hydrochloric acid (5 L), and once with methanol (2 L). The filter cake was dried at 70-80° C. to obtain 61.3 g of a white pentaerythritol tetrabenzenesulfonate powder product, with a yield of 92% and a melting p...

Embodiment 2

[0029] Add 1.8L of pyridine into a 5L three-necked flask with magnetic stirring and cool to 0°C, add 593g (2.26mol) of dibromoneopentyl glycol under stirring, and then add p-toluenesulfonyl chloride (1kg) in batches, and the temperature will rise slowly for 20 minutes After the addition, the temperature rose to 20°C, and after the addition, it was moved to room temperature for 12 hours of reaction. The above reaction solution was slowly added dropwise to 2.5L of ice water with stirring, and the temperature was controlled not to exceed 40°C during the dropwise addition, and then filtered, and the filter cake was washed successively with 2N hydrochloric acid (1L), and washed with water until neutral. Then 2L of ethanol was rinsed, and the filter cake was dried to obtain 1314g of product, and the yield was greater than 100%.

[0030] Weigh 4mol of the above-mentioned intermediate, 1266g (3eq) of sodium bromide, and 8.5L of diethylene glycol in a 20L three-necked flask. Add 10L o...

Embodiment 3

[0032] Add 9.6 mol of dibromoneopentyl glycol and 6.5 L of pyridine into a 20 L three-necked flask, and add 21 mol of benzenesulfonyl chloride dropwise under stirring. Control the rate of addition to keep the reaction temperature below 35°C, and drop it in 1.2 hours. After the dropwise addition, the stirring reaction was continued at 30° C. for 4 h. After the reaction was completed, the cold bath was cooled to 2 ° C, and then the above reaction system was added dropwise to 5 L of ice water, and the temperature was controlled to be lower than 40 ° C during the dropping process, and a white granular precipitate was formed. After filtering, the filter cake was washed twice with water (5 L×2), once with 5% hydrochloric acid (5 L), and once with methanol (2 L). The filter cake was dried at 70-80°C to obtain the activated product with a yield of 91.5%.

[0033] Add 12.6mmol of dried activated product, 20ml of diethylene glycol (DEG), 0.75g (1.25mmol) of polyethylene glycol (PEG600...

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

No PUM Login to view more

Abstract

The invention discloses a synthetic method of tetrabromo neopentane. The method is characterized by: adopting pentaerythritol or dibromo neopentyl glycol or tribromo neopentyl alcohol as the raw material to react with methylsulfonyl chloride or p-toluenesulfonyl chloride to perform hydroxyl activation, and then taking diethylene glycol or polyethylene glycol as the solvent and using polyethylene glycol as the catalyst, carrying out substitution reaction with sodium bromide to obtain tetrabromo neopentane; or taking dibromo neopentyl glycol or tribromo neopentyl alcohol as the raw material, firstly reacting with p-toluenesulfonyl chloride to carry out hydroxyl activation, and then taking diethylene glycol as the solvent to carry out substitution reaction with sodium bromide to obtain tetrabromo neopentane. The whole process avoids the generation of water vapor, controls the temperature easily, and is environment-friendly, high in yield and good in product purity.

Description

technical field [0001] The invention relates to a synthesis method of tetrabromoneopentane, which belongs to the technical field of organic synthesis. Background technique [0002] Tetrabromoneopentane is also known as pentaerythrobromide. Molecular formula C 5 h 8 Br 4 Molecular weight 387.73. [0003] Tetrabromoneopentane is an important intermediate for the synthesis of water-based adhesive cross-linking agents and other dendrimers (or oligomers) and surfactants, and the development and application of these products have significant environmental and social benefits and economic benefits. Therefore, improving the synthetic method of tetrabromoneopentane has certain practical significance. [0004] There are two main traditional synthesis methods of tetrabromoneopentane. The first is the reaction bromination of pentaerythritol and phosphorus tribromide to obtain the target product. Due to the moisture absorption and other properties of phosphorus tribromide in this ...

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
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C07C17/093C07C19/075C07C303/28C07C309/73
CPCC07C17/093C07C303/28C07C309/73C07C19/075
Inventor 刘殿卿
Owner CHONGQING MEDICAL & PHARMA COLLEGE
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap