Preparation method of phosphite ester by using dividing wall tower reaction rectification technique

A technology of reactive distillation and phosphite, which is applied in the field of intermediates and fine chemical additives, can solve the problems of poor operating environment, many by-products, and difficult purification of products, and achieve the effect of fast reaction rate and reduction of by-products

Inactive Publication Date: 2010-07-14
QINGDAO UNIV +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, phosphorus trichloride is volatile, highly toxic, and the operating environment is poor. The key is that there are many by-products. In order to reduce side reactions, it is often necessary to add

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0033] Example 1

[0034] For the preparation of tributyl phosphite, the reaction temperature in the early stage is 120℃, and the temperature is gradually increased to 160℃ in the later stage.

[0035] The amount of raw materials and their corresponding substances are as follows:

[0036] ① Phosphorous acid 82

[0037] ②N-butanol 660

Example Embodiment

[0038] Example 2

[0039] For the preparation of dibutyl phosphite, the reaction temperature in the early stage is 120℃, and the temperature is gradually increased to 150℃ in the later stage.

[0040] The amount of raw materials and their corresponding substances are as follows:

[0041] ① Phosphorous acid 82

[0042] ②N-butanol 300

Example Embodiment

[0043] Example 3

[0044] For the preparation of diethyl phosphite, the reaction temperature is 80℃ in the early stage, and the temperature is gradually increased to 110℃ in the later stage.

[0045] The amount of raw materials and their corresponding substances are as follows:

[0046] ① Phosphorous acid 82

[0047] ②Ethanol 280

[0048] ③Benzene 80

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PUM

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Abstract

The present invention discloses a preparation method of phosphite ester by using a dividing wall tower reaction rectification technique, comprising the following steps: selecting phosphorous acid, a reactant alcohol and a water carrying agent as raw materials, the dosage of the reactant alcohol is 2 to 9 times the demand of the reaction; adding the raw materials into a reactor which is additionally provided with a dividing wall-typed rectifying tower for reaction, the reaction temperature is between 80 to 160 DEG C, leading cooling water into the overhead condenser timely, distilling off the lowest binary azeotrope formed by the water of the reaction and the reactant alcohol or the lowest ternary azeotrope formed by the water of the reaction, the reactant alcohol and the water carrying agent from the tower top, leading the distillate into a stratifying device after condensation, leading the oil phase into the side communicated with the reactor and leading the aqueous phase into the other side; stopping the backflow when the amount of the water in the aqueous phase reaches the preconcerted amount, distilling off the excessive reactant alcohol; stopping the heat when no distillate appears on the tower top, and the product let out from the tower bottom is phosphite ester. The invention has fast reaction speed, high product purity and fewer by-products.

Description

Technical field [0001] The invention belongs to the technical field of fine chemical additives and intermediates, and relates to an improved preparation method of phosphites. Background technique [0002] At present, the production of phosphites in the field of fine chemical additives and intermediates uses volatile phosphorus trichloride and corresponding alcohols as raw materials. Many processes also use toluene as solvents at 50-70°C. Reaction at low temperature. When the alcohol is excessive, the phosphite triester and a large amount of hydrogen chloride and the by-product chloroalkane are obtained. When the amount of alcohol is insufficient and the phosphite triester can be decomposed into the phosphite diester and the corresponding chloroalkane in the presence of hydrogen chloride, after the reaction is completed, The hydrogen chloride and chloroalkane produced by the reaction are distilled off, and then the corresponding phosphite is obtained by vacuum distillation, and h...

Claims

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Application Information

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IPC IPC(8): C07F9/141C07F9/142
Inventor 聂兆广胡艳芳王兆俊李志国杜万军
Owner QINGDAO UNIV
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