Check patentability & draft patents in minutes with Patsnap Eureka AI!

Preparation method for 2,5-furandimethanoldialkyl ether

A technology of furandimethanol dialkyl ether and furandimethanol dibutyl ether, which is applied in the field of preparation of 2,5-furandimethanol dialkyl ether, can solve the problems of high production cost, environmental pollution by waste residue and waste liquid, corrosion To eliminate candles and human health hazards, achieve the effects of reducing waste liquid and waste residue, high selectivity, and reducing rotten candles

Inactive Publication Date: 2019-06-07
DONGGUAN UNIV OF TECH +1
View PDF4 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to the high production cost of HMF, since the 1980s, HMF has not yet been industrialized. The efficient conversion and utilization of HMF has become one of the difficulties in scientific research, which has led to the development of 2,5-furan di The production and application of a series of disubstituted furan derivatives such as methanol dialkyl ether have been greatly restricted
[0003] The existing patent CN103058962A discloses a preparation method of 2,5-furandimethanol dialkyl ether, but the method in this patent uses a homogeneous acid catalyst such as sulfuric acid. The common disadvantage of these liquid catalysts is that the production equipment Corrosion candles and human health are seriously endangered, and a large amount of waste residue and waste liquid will be produced to pollute the environment

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0040] (1), the Fe 2 o 3 -CoO 2 -CuO 2 / ZrO 2 The supported catalyst was added to 50 mL of formaldehyde solution with a mass fraction of 37%, mixed evenly, added 5 mL of furfuryl alcohol, and reacted for 60 h in an oil bath with magnetic stirring at 35 ° C. After cooling to room temperature, it was analyzed by high performance liquid chromatography (HPLC). ) analysis, furfuryl alcohol conversion rate and 2,5-furan dimethanol selectivity were 74% and 63% respectively, under reduced pressure distillation at 80 ℃, formaldehyde solution and unreacted furfuryl alcohol were removed, and brownish yellow crude 2,5-furan dimethanol was obtained. methanol liquid. where Fe 2 o 3 -CoO 2 -CuO 2 / ZrO 2 The weight ratio of supported catalyst to furfuryl alcohol is 0.2:1.

[0041] (2), take 8.5 g of 2,5-furandimethanol prepared in the above step (1), dissolve it with 124 mL of butanol, and then add Fe 2 o 3 -CoO 2 -CuO 2 / ZrO 2 Supported catalyst, where Fe 2 o 3 -CoO 2 -CuO ...

Embodiment 2

[0043] (1), the Fe 2 o 3 -CoO 2 -CuO 2 / ZrO 2 The supported catalyst was added to 50 mL of formaldehyde solution with a mass fraction of 37%, mixed evenly, added 5 mL of furfuryl alcohol, and reacted for 60 h in an oil bath with magnetic stirring at 35 ° C. After cooling to room temperature, it was analyzed by high performance liquid chromatography (HPLC). ) analysis, furfuryl alcohol conversion rate and 2,5-furan dimethanol selectivity were 74% and 63% respectively, under reduced pressure distillation at 80 ℃, formaldehyde solution and unreacted furfuryl alcohol were removed, and brownish yellow crude 2,5-furan dimethanol was obtained. methanol liquid. where Fe 2 o 3 -CoO 2 -CuO 2 / ZrO 2 The weight ratio of supported catalyst to furfuryl alcohol is 0.2:1.

[0044] (2) Take 8.5 g of 2,5-furandimethanol prepared in the above step (1), dissolve it in 124 mL of methanol, and then add Fe 2 o 3 -CoO 2 -CuO 2 / ZrO 2 Supported catalysts where Fe 2 o 3 -CoO 2 -CuO 2...

Embodiment 3

[0046] (1), the Fe 2 o 3 -CoO 2 -CuO 2 / ZrO 2 The supported catalyst was added to 50 mL of formaldehyde solution with a mass fraction of 37%, mixed evenly, added 5 mL of furfuryl alcohol, and reacted for 60 h in an oil bath with magnetic stirring at 35 ° C. After cooling to room temperature, it was analyzed by high performance liquid chromatography (HPLC). ) analysis, furfuryl alcohol conversion rate and 2,5-furan dimethanol selectivity were 74% and 63% respectively, under reduced pressure distillation at 80 ℃, formaldehyde solution and unreacted furfuryl alcohol were removed, and brownish yellow crude 2,5-furan dimethanol was obtained. methanol liquid. where Fe 2 o 3 -CoO 2 -CuO 2 / ZrO 2 The weight ratio of supported catalyst to furfuryl alcohol is 0.2:1.

[0047] (2), take 8.5g of 2,5-furandimethanol prepared in the above step (1), dissolve it with 124mL decanol, and then add Fe 2 o 3 -CoO 2 -CuO 2 / ZrO 2 Supported catalysts where Fe 2 o 3 -CoO 2 -CuO 2 / Z...

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 preparation method for 2,5-furandimethanoldialkyl ether. According to the novel method for preparing the 2,5-furandimethanoldialkyl ether, provided by the invention, homogeneous acid catalysts including sulfuric acid and the like are not used, so that the corrosion to protection equipment and the endangering degree to human bodies are effectively reduced; and meanwhile, waste liquid and waste residues, which are produced in a production process, are reduced, so that the method is an environment-friendly novel method. Moreover, the novel method for preparing the 2,5-furandimethanoldialkyl ether, provided by the invention, has the advantages that the conversion rate of 2,5-furandimethanol and the selectivity of the 2,5-furandimethanoldialkyl ether are higher than those in the prior art.

Description

technical field [0001] The invention belongs to the field of organic synthesis, and in particular relates to a preparation method of 2,5-furandimethanol dialkyl ether. Background technique [0002] Furanylmethanol dialkyl ether is a new type of diesel additive, which can significantly increase the cetane number of diesel. The traditional synthesis method of 2,5-furandimethanol dialkyl ether is to use 5-hydroxymethylfurfural (HMF) as the substrate and prepare it through selective hydrogenation and etherification. For example, Gruter et al reported in the patent (EP2008 / 007423) that 5-hydroxymethylfurfural or 5-alkoxymethylfurfural can be converted into furandimethanol dialkyl under the condition that hydrogenation catalyst and acidic catalyst exist simultaneously ether. However, due to the high production cost of HMF, since the 1980s, HMF has not yet been industrialized. The efficient conversion and utilization of HMF has become one of the difficulties in scientific researc...

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
IPC IPC(8): C07D307/60B01J23/75
Inventor 李燕茜李豫珍
Owner DONGGUAN UNIV OF TECH
Features
  • R&D
  • Intellectual Property
  • Life Sciences
  • Materials
  • Tech Scout
Why Patsnap Eureka
  • Unparalleled Data Quality
  • Higher Quality Content
  • 60% Fewer Hallucinations
Social media
Patsnap Eureka Blog
Learn More