The manufacture method of fluoroalkyl iodide

A technology for fluoroalkyl iodides and manufacturing methods, which is applied in the fields of chemical instruments and methods, organic chemistry, preparation of halogenated hydrocarbons, etc., and can solve the problems of increasing reactors, reducing reaction speed, and reducing the selectivity of fluoroalkyl iodides, etc. problems, to achieve the effects of shortened residence time, increased reaction speed, and excellent reaction efficiency

Active Publication Date: 2016-05-18
DAIKIN IND LTD
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Although this production method is also an excellent production method, since the telomerization reaction is a gas-liquid reaction, when the contact efficiency between the gas phase and the liquid phase is low, there is a problem that the reaction rate decreases
When the reaction speed decreased, a stepwise reaction took place in the reactor due to a long residence time, and the chain length of the obtained fluoroalkyl iodide became longer, thus, there was, for example, 1-iodoperfluorohexane (C 6 f 13 I, degree of polymerization n=2), 1-iodoperfluorooctane (C 8 f 17 I, the degree of polymerization n=3) etc., the problem that the selectivity of the desired fluoroalkyl iodides with a degree of polymerization n of 2 or more decreases
[0006] In addition, in order to ensure a predetermined throughput, the gas-liquid contact area must be increased to improve the contact efficiency between the gas phase and the liquid phase, and there is a problem that the equipment of the reactor must be increased.
Therefore, the above-mentioned production method cannot be said to be a method capable of satisfying industrial requirements.

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
  • The manufacture method of fluoroalkyl iodide
  • The manufacture method of fluoroalkyl iodide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0075] use as figure 1 The reaction apparatus shown is for telomerization reaction. In a stainless steel pressurized reactor 1 with a capacity of 3 L with a stirrer 2, 1-iodoperfluorobutane (C 4 f 9I) 3.0 kg and 150 g of copper powder as a metal catalyst were stirred by the stirrer 2 . It was circulated by the circulation pump 3, and it heated to 100 degreeC. While maintaining the temperature in the reactor at 100° C., tetrafluoroethylene as the main chain product was supplied to the injector 8 through the piping for feeding the raw material main chain product. Stirring the reaction liquid, the pressure was increased until the pressure in the reactor reached 0.38 MPa (gauge pressure).

[0076] Afterwards, keep above-mentioned temperature and pressure condition, feed 1-iodoperfluorobutane (C 4 f 9 I) Copper powder as a metal catalyst was supplied to the reaction liquid circulation pipe 7 at a flow rate of 150 g / hr. And, supply tetrafluoroethylene to injector 8 with the f...

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 present invention provides a novel preparation method of fluoroalkyl iodile, which can prepare fluoroalkyl iodile with high selection rate, and furthermore a small-size reactor can be used and excellent production efficiency is obtained. Particularly the invention provides the preparation method of the fluoroalkyl iodile, which is characterized in that: in a reactor, telomerization between fluoroalkyl iodile which is used as telogen and is represented by a formula (I) and tetrafluoroethylene that is used as backbone material is caused for preparing the fluoroalkyl iodile represented by the formula (II). In the RfI formula (I), Rf is a fluoroalkyl of which the number of carbon atoms is 1-6. In the Rf-(CF2CF2)n-I formula (II), Rf is same with that in the formula (I), and n is an integer selected from 1-4. Reaction solution in the reactor is extrated and is fed from an ejector inlet on the reactor to the inner part of the ejector. When the reaction solution passes through the ejector, gas which contains tetrafluoroethylene in the reactor is sucked from the suction port of the ejector to the inner part of the ejector. Mixture of the reaction solution and the gas which comprises tetrafluoroethylene is sprayed from the outlet of the ejector into the reactor, thereby causing reaction between the fluoroalkyl iodile represented by the formula (I) and tetrafluoroethylene.

Description

technical field [0001] The present invention relates to a method for producing fluoroalkyl iodides. Background technique [0002] Conventionally, there is known a method for producing fluoroalkyl iodides by telomerization. [0003] In such a telomerization reaction, 1-iodoperfluoroethane (C 2 f 5 I) A fluoroalkyl iodide is produced by stepwise reaction with tetrafluoroethylene as a main chain (for example, refer to Patent Document 1). [0004] In such a method, 1-iodoperfluoroethane (C 2 f 5 I) The reaction liquid obtained by reacting with tetrafluoroethylene exists as a liquid phase, and tetrafluoroethylene is supplied in a gas phase adjacent to the liquid to further promote the production of fluoroalkyl iodides. [0005] Although this production method is also an excellent production method, since the telomerization reaction is a gas-liquid reaction, there is a problem that the reaction rate decreases when the contact efficiency between the gas phase and the liquid ph...

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 Patents(China)
IPC IPC(8): C07C19/16C07C17/278
Inventor 平坂岳臣市田卓也长谷川知邦
Owner DAIKIN IND LTD
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