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Preparation method of DL-proline

A technology of proline and glacial acetic acid, applied in the field of preparation of DL-proline, can solve the problems of easily affecting product quality, long production cycle, inconvenient industrial operation and the like

Active Publication Date: 2020-10-27
SUZHOU YUANFANG CHEM
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] The preparation of DL-proline in the prior art requires many process steps, which will cause more uncontrollable factors, which will easily affect the quality of the product and reduce its market competitiveness.
And the preparation method of DL-proline in the prior art has a long production cycle, high input cost, and is not convenient for industrialized operation

Method used

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  • Preparation method of DL-proline
  • Preparation method of DL-proline

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] 100 g of glacial acetic acid was put into the reactor, and 100 g of L-proline was added under stirring to obtain a reaction solution. Stir the reaction solution to heat up to 70-75°C, and keep stirring for 3 hours to make the racemization reaction of L-proline fully occur, so that the optical rotation of the reaction solution is 0, and the reaction solution is reddish brown at this time.

[0035] After cooling the reaction solution with optical rotation of 0 to 30°C, move it to a distillation pot for distillation under reduced pressure. The distillation temperature is 55-60°C, and the vapor pressure is 0.1MPa. Continue to distill for 30 minutes after distillation until no liquid flows out. The residue after distillation was concentrated to 10% of the original volume to obtain viscous concentrate A.

[0036] Mix the concentrated solution A with 120 g of isopropanol, stir until the crystals are completely precipitated, then cool down to 15°C, centrifuge to remove excess l...

Embodiment 2

[0040] Put 200 g of glacial acetic acid into the reaction kettle, and then add 100 g of L-proline under stirring to obtain a reaction solution. Stir the reaction solution to heat up to 70-75° C., then keep warming and stirring for 3 hours, so that the optical rotation of the reaction solution is 0, and the reaction solution is reddish-brown at this time.

[0041] After cooling the reaction solution with optical rotation of 0 to 30°C, move it to a distillation pot for distillation under reduced pressure. The distillation temperature is 55-60°C, and the vapor pressure is 0.1MPa. Continue to distill for 30 minutes after distillation until no liquid flows out. The residue after distillation was concentrated to 10% of the original volume to obtain viscous concentrate A.

[0042] Mix the concentrated solution A with 120 g of isopropanol, stir until the crystals are completely precipitated, then cool down to 15°C, centrifuge to remove excess liquid, rinse the crystals with isopropano...

Embodiment 3

[0046] Put 80 g of glacial acetic acid into the reaction kettle, and then add 100 g of L-proline under stirring to obtain a reaction solution. Stir the reaction solution to heat up to 70-75°C, keep stirring for 6 hours, and then cool to 30°C.

[0047] Move the reaction solution cooled to 30°C to a still pot for distillation under reduced pressure. The distillation temperature is 55-60°C and the vapor pressure is 0.1MPa. Continue to distill for 30 minutes after distillation until no liquid flows out, and then distill the residue after distillation Concentrate to 10% of the original volume to obtain viscous concentrate A.

[0048] Mix the concentrated solution A with 120 g of isopropanol, stir until the crystals are completely precipitated, then cool down to 15°C, centrifuge to remove excess liquid, rinse the crystals with isopropanol to obtain a crude product.

[0049] Mix 90 g of the crude product, 5 g of activated carbon, and 185 g of water, stir and raise the temperature to...

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Abstract

The invention discloses a preparation method of DL-proline, which comprises the following steps: mixing L-proline and glacial acetic acid, stirring and heating the mixture to 60-75 DEG C, stirring themixture for 2-6 hours while keeping the temperature, and distilling the mixture to obtain the DL-proline, wherein the distillation method comprises the following steps: distilling until no liquid flows out, and continuously distilling for 20-40 minutes; concentrating residues after distillation to obtain a concentrated solution A; mixing the concentrated solution A with isopropanol, stirring until crystals are completely separated out, collecting the crystals, and rinsing with isopropanol to obtain a crude product; mixing and stirring the crude product, activated carbon and water until the crude product is completely dissolved, filtering to remove the activated carbon, and concentrating the filtered residues to obtain a concentrated solution B; mixing the concentrated solution B with isopropanol, performing stirring until crystals are completely separated out, collecting the crystals, performing rinsing with isopropanol, and after rinsing, drying the crystals so as to obtain DL-proline. The preparation method of the DL-proline is simple in process and convenient for industrial operation, and the yield and quality of the product are improved.

Description

technical field [0001] The invention relates to the field of biotechnology, in particular to a preparation method of DL-proline. Background technique [0002] DL-proline is widely used in the fields of food and medicine, and can be used as nutritional additives and pharmaceutical raw materials. [0003] The preparation of DL-proline in the prior art requires numerous process steps, which will cause more uncontrollable factors, which will easily affect the quality of the product and reduce its market competitiveness. Moreover, the preparation method of DL-proline in the prior art has a long production cycle, high input cost, and is not convenient for industrial operation. [0004] Therefore, it is necessary to propose a new preparation method of DL-proline to simplify its processing steps, improve processing efficiency and product quality, and reduce processing costs. Contents of the invention [0005] In order to overcome the defects in the prior art, the embodiment of t...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07D207/16
CPCC07D207/16C07B2200/13
Inventor 张小峰
Owner SUZHOU YUANFANG CHEM