Method of producing 2-chlorbutadiene-1,3

专利摘要:
Improvement in the catalytic dehydrohalogenation of a halogenated hydrocarbon to an ethylenically unsaturated product with aqueous alkali in a series of reactors in a cascade arrangement, wherein the fresh alkali feed is relocated from the first reactor to a reactor subsequent to the first, and partly spent alkali solution from the last reactor is recirculated to the first reactor, while the ethylenically unsaturated product is recovered from the effluent from the last reactor, and waste brine is removed from the effluent from the reactor immediately preceding that to which fresh alkali is fed. In this manner, the amount of both the alkali and the catalyst can be reduced, and the conversion is increased. Dehydrochlorination of 3,4-dichlorobutene-1 gives chloroprene, which is a valuable monomer for making synthetic elastomers.
公开号:SU1277888A3
申请号:SU833666211
申请日:1983-11-28
公开日:1986-12-15
发明作者:Джозеф Морин Ш. Луи
申请人:Е.И.Дюпон Де Немур Энд Компани (Фирма)；
IPC主号:

专利说明:

The invention relates to a process for the preparation of 2-chlorobutadiene 1.3 of one of the most important monomers in the main organic synthesis industry in the preparation of sex materials. The purpose of the invention is to reduce the consumption of catalyst and alkali, increase the degree of conversion of the starting 3,4-dichlorobutene-1 (DCB). Figure 1 shows a diagram of a known method using several installed reactors; in the form of a cascade; figure 2 - diagram of one of the variants of the proposed method; fig.Z - the same with the use of two reactors. In a preferred embodiment, the reactor is made of a corrosion-resistant material or is lined with this material, for example, nickel. Reactors are provided with appropriate heating and cooling devices and mixing devices. In a known method (Fig.), The steps are carried out in diagrams R 2 , R, and K, a mixture of the catalyst with the initial halogenated hydrocarbon is fed to R via line 1, and the aqueous solution is fed and fed through line 2. The flow from each stage is directed into the next stage, and the stream flowing from the last stage is separated into the organic phase and the aqueous phase in a sump D ,, the product saturated with ethylene is removed from the organic phase, the waste is removed via line 3, and the spent brine is removed via line 4. In FIG. . 2 shows one variant of the proposed method, where a mixture of the catalyst with DCB is fed along line 1. A fresh aqueous solution of the first stage R is fed to the reactor with an alkali R through line 2. The stream from the reactor R is introduced into the reactor-R 5 and the stream from the reactor R is divided into phases in a sump D. Chloroprene is removed from the organic phase and withdrawn t along line 3, while the aqueous phase containing a mixture of sodium hydroxide vi sodium chloride through line 4 serves iia the first stage. The flow from the reactor R. in the settling tank 1) the organic phase is divided, in the case considered, containing DCB and chloropen and the aqueous phase, which is the spent brine. The organic phase is fed through line 5 to stage R, and the spent solution is withdrawn through line 6. FIG. 3 shows a two-reactor process diagram. Catalyst mixture with halogenated; hydrocarbon line 1 is served on the first stage R ,. Fresh water; an alkaline creature fed through line 2 is combined with the upper phase of sump D containing a mixture of DCB. The combined two-phase mixture is introduced into the reactor R, and the effluent from the reactor R is divided into phases in sump D. On the other hand, a fresh alkaline aqueous solution can be fed directly to the reactor R according to the method shown in Fig. 2. The organic phase, discharged via line 4, contains mainly chloroprene. The aqueous phase, consisting of a mixture of alkali metal hydroxide and brine, is fed to the reactor R, via line 5, the spent oassol is withdrawn from the bottom of the sump D, through line 6 and discarded. According to the proposed method, a higher conversion of dBB to chloroprene is obtained, which is by a known method. At the same time, a smaller amount of catalyst and alkali is required than in a known process, since the driving forces of the reaction are more randomly distributed across the available reactor volumes, thereby yielding significant savings. The preferred point of entry of fresh alkali is approximately at the midpoint of the reactor chain, however, most of the advantages of this invention will also be achieved if a solution of fresh alkali is supplied to some other stage between the percy reactor and the latter. With the exception of the location of the feed and discharge streams and the consumption of alkali costs and catalysis, other conditions of process 5, temperature and flow rates 5 remain essentially the same as in the known method. The invention is illustrated by the following examples in which all parts of the quantity and percentages are by weight, unless otherwise specified. Example 1. In this example, experiment A was carried out in accordance with the well-known method shown in Fig. 1, while experiment B was carried out in accordance with the present invention (temperature 60 ° C. In each case, three nickel reactors with a volume of 1650 ml were used with back stirring. At the first stage, 0.918 kg / h of DHB containing 2500 ppm of catalyst concentration, 0.025% by weight of DHB cocobenzylbis (γ9-hydroxypropyl) ammonium chloride is served. The aqueous alkali solution is a fresh 22% NaOH solution in water. In experience A, the molar ratio of NaOH to DCB is 1.058; This ratio C was equal to 1.064. The degree of conversion of DHB at each stage for each experiment was determined by gas chromatography.The results of the experiments are given in the following Table I. Table 1
Fresh alkali feed stage
Table 84 using known equipment. The process parameters as well as the results were calculated for the process using eight liquid-filled, back-mixed reactors connected in series. The catalyst was the same as in example 1, and the consumption of DHB was 16,589 kg / h. The results of the experiments are given in table. 2 and 3. Table. Concentration in water,% Molar ratio NaOH / DCB. Concentration of the catalyst in the initial 2420 DCB, ppm - ppm (%) 1060 (0,0106) (0,024)
It can be noted that in experiment B, the amount of unconverted DHB at stage 3 is so small that it actually amounts to about zero. This result indicates that a large driving force is provided, since there is a higher alkali concentration in the last reaction steps.
PRI mme R 2. The temperature in the reactor at all stages is equal.
This example simulates the operation of an industrial plant based on the known kinetics of reaction with
The output of chloroprene%.
99.7
99.6
512
The above data shows that when operating in accordance with the proposed method, the amount of catalyst and excess fresh alkali decrease, while the degree of conversion of DCB and the yield of chloroprene slightly increase.
Example 3. Experiments were carried out on a pilot plant using four liquid-filled reactors with backmixing and using the same catalyst as in Example 1. DHB is supplied at a rate of 4310 kg / h, as a fresh aqueous alkali solution. a 20.5% sodium hydroxide solution is used; Other process conditions and results are shown in Tables 4 and 5.
Table 4 The molar ratio of NaOH / DHB1.064 The concentration of catalyst in the Supplied DCB, ppm (%) 2100 (0.02 Unconverted DCB after the last stage (% of initial amount) 0.73
Continuation of table 4
,
Phie2 The temperatures in the reactors were as follows: in experiment E 60 C at all stages, in experiment F at all stages, except for 2, at the second stage 65 C. The concentration of catalyst in experiment E was 0.021% and in experiment F 0 , 0112% by weight of DHB in raw materials. The amounts of both sodium hydroxide and catalyst were reduced, but at the same time both the degree of conversion of DHB and the yield of chloroprene increased when the supply of fresh water in the second stage was switched to the third stage,
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权利要求:
Claims (2)
[1]
METHOD FOR PRODUCING
[2]
2-CHLOROBUTADIENE-1,3 by dehydrochlorination of 3,4dichlorobutene-1 with an aqueous alkali solution at 60-65 ° C in the presence of a quaternary ammonium base catalyst, cocobenzylbis (β-hydroxypropyl) ammonium chloride in several reactors in series, characterized in that, for the purpose of reducing the consumption of catalyst and alkali, increasing the degree of conversion of the starting 3,4-dichlorobutene-1, the process is carried out in 2-8 consecutive reactors, while 3,4-dichlorobutene-1 and the catalyst are fed into the first reactor, and a fresh aqueous solution of alkali under they are fed into the reactor following the first one, and it can be supplied together with the organic phase entering this reactor, the reaction mass from the last reactor is stratified into a partially spent aqueous alkali solution, which is fed into the first reactor, and the organic phase from which the target product is removed, and the spent aqueous alkali solution is removed from the reactor before the feed point of the fresh aqueous alkali solution.
SU <„1277888 AZ

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同族专利:

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引用文献:

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US3981937A|1966-06-03|1976-09-21|E. I. Du Pont De Nemours And Company|Dehydrohalogenation of 3,4-dichloro-1-butene|

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US3754044A|1968-02-28|1973-08-21|Du Pont|Dehydrohalogenation of halogenated compounds|JPH0457657B2|1985-12-23|1992-09-14|Mitsui Toatsu Chemicals|

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US5237114A|1992-03-20|1993-08-17|E. I. Du Pont De Nemours And Company|Removal of catalyst from chloroprene by treatment with oxy acid|

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CA2152940C|1992-12-29|1998-05-05|Seiji Takubo|A method of producing 1,1,1,3,3-pentafluoropropane, a method of producing 1,1,1,3,3-pentafluoro-2-halogeno-3-chloropropane, and a method of producing 1,1,1,2,3,3-hexachloropropene|

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US5396002A|1993-08-18|1995-03-07|The Dow Chemical Company|Process to produce vinylidene chloride using phase transfer catalyst|

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US6380446B1|2000-08-17|2002-04-30|Dupont Dow Elastomers, L.L.C.|Process for dehydrohalogenation of halogenated compounds|

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ITMI20052455A1|2005-12-22|2007-06-23|Solvay Solexis Spa|PROCEDURE FOR THE PREPARATION OF FLUOROALOGENOETERI|

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ITMI20052456A1|2005-12-22|2007-06-23|Solvay Solexis Spa|PROCEDURE FOR THE PREPARATION OF FLUOROALOGENOETERI|

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JP2010229092A|2009-03-27|2010-10-14|Tokuyama Corp|Method for producing trichloropropene|

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US8969645B2|2012-12-14|2015-03-03|Chevron U.S.A. Inc.|Process for reducing chloride in hydrocarbon products using an ionic liquid catalyst|

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JP5900671B2|2014-04-28|2016-04-06|ダイキン工業株式会社|Process for producing 1,1,2-tribromoethane|

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WO2015166961A1|2014-04-28|2015-11-05|ダイキン工業株式会社|1,1,2-tribromoethane production method|

法律状态:

优先权:

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申请号 | 申请日 | 专利标题

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US06/445,155|US4418232A|1982-11-29|1982-11-29|Dehydrohalogenation process|

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