Purification method of high-purity fluorescein

A purification method and technology of fluorescein, which is applied in the field of fluorescein purification, can solve the problems that it is difficult to obtain high-purity fluorescein, and achieve the effects of easy reduction, easy preparation, and good crystallinity

Pending Publication Date: 2021-10-01
山东绅联药业股份有限公司
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Therefore, it is difficult to obtain high-purity fluorescein by conventional processes

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
  • Purification method of high-purity fluorescein
  • Purification method of high-purity fluorescein
  • Purification method of high-purity fluorescein

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] The crude fluorescein obtained by co-heating phthalic anhydride and resorcinol is used as a raw material. The purity of the raw material is not limited, and the conventional crude fluorescein obtained in industry is sufficient. Take 25g of crude fluorescein and 125ml of glacial acetic acid in a 500mL three-necked reaction bottle, stir evenly at 80-100 rpm, then take a sample and spot the plate to obtain the following: figure 1 For the reaction point shown, continue to add 5g of pyridine (acid-binding agent) and 10g of acetic anhydride into the reaction bottle, control the temperature at 50-60°C and stir the reaction for 3h at a speed of 80-100rpm, and continue to take samples and spot the plate to obtain the following: figure 1 As shown in the product point, TLC monitors developing agent 1ml ethyl acetate plus 2ml petroleum ether, diacetyl fluorescein Rf = 0.8, the reactant crude fluorescein Rf = 0.5, the product point has no crude fluorescein, it proves that the reactio...

Embodiment 2

[0048] The parts of this embodiment that are not specifically described are consistent with Embodiment 1.

[0049]Take 100g of crude fluorescein and 500ml of glacial acetic acid in a 1L three-necked reaction flask, stir evenly, add 20g of pyridine and 40g of acetic anhydride, stir at a temperature of 50-60°C for 3 hours, monitor the reaction result by TLC, add 2ml of ethyl acetate to 1ml of developer Petroleum ether produces diacetyl fluorescein Rf = 0.8, and the crude fluorescein Rf = 0.5. After the reaction was complete, the temperature was lowered to below 25°C, stirred and crystallized for 1 hour, and suction filtered. The filter cake was beaten once with 500ml of purified water, and dried at 50°C by blowing air to obtain 112g of orange-yellow diacetylfluorescein. Dissolve with 5 times the volume of dichloromethane at 40°C, add 5 times the volume of diethyl ether to precipitate, cool to 0-5°C and stir for 1 hour, then filter with suction, and air-dry at 50°C to obtain 101 ...

Embodiment 3

[0054] The parts of this embodiment that are not specifically described are consistent with Embodiment 1.

[0055] Take 3kg of crude fluorescein and 15L of glacial acetic acid in a 50L glass reactor, stir evenly, add 600g of pyridine and 1.2kg of acetic anhydride, stir at a temperature of 50-60°C for 3 hours, monitor the reaction results by TLC, add 1ml of ethyl acetate as a developer 2ml of petroleum ether produces diacetyl fluorescein Rf=0.8, and the crude fluorescein Rf=0.5. After the reaction was complete, the temperature was lowered to below 25°C, stirred and crystallized for 1 hour and suction filtered. The filter cake was beaten once with 15 L of purified water, and air-dried at 50°C for 8 hours to obtain 3.40 kg of orange-yellow diacetyl fluorescein. Dissolve with 5 times the volume of dichloromethane at 40°C, add 5 times the volume of diethyl ether to precipitate, cool to 0-5°C and stir for 1 hour, then filter with suction, and air-dry at 50°C to obtain 3.05kg of whit...

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

PropertyMeasurementUnit
wavelengthaaaaaaaaaa
Login to view more

Abstract

The invention belongs to the technical field of fluorescein purification, and relates to a purification method of high-purity fluorescein. The method takes crude fluorescein as a raw material, and is characterized in that pure water pulping and recrystallization are carried out after acetylation reaction, and then sodium methoxide is used for deacetylation refining to obtain refined fluorescein. The invention relates to a novel process for purifying fluorescein by utilizing a method for preparing a fluorescein derivative. Fluorescein diacetate is easy to prepare and reduce, has very good crystallinity and is greatly different from the impurities in property, so that the problems of repeated use of acid and alkali and coprecipitation of the impurities and fluorescein in the prior art are solved by a purification route of preparing fluorescein diacetate from fluorescein sodium and then carrying out saponifying and reducing.

Description

technical field [0001] The invention belongs to the technical field of fluorescein purification and relates to a method for purifying high-purity fluorescein. Background technique [0002] Fluorescein (fluorescein) is also known as fluorescent orange or fluorescent orange red, and its chemical name is 3',6'-dihydroxyspiro[isobenzofuran 1 ( 3H),9'-(9H)-xanthene]-3-one or 9-(O-carboxyphenyl)-6-hydroxy-3H-xanthene-3-one, first synthesized by VonBayer in 1871. Fluorescein has three interconversion structures: lactone structure, quinone structure, and zwitterion structure. The molecular structure is as follows: [0003] [0004] The maximum absorption / emission wavelength of fluorescein is at 492 / 571 nm (in water), and the fluorescence quantum yield is at 0.92 (pH>8). Due to the existence of oxygen bridge bonds, the two benzene rings are fixed on a plane, so that the molecule has a rigid coplanar structure, which can produce strong fluorescence under the action of excitati...

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 Applications(China)
IPC IPC(8): C07D311/82C07D493/10
CPCC07D311/82C07D493/10
Inventor 张兆元高云兵甄爱华刘建洋苗元旭
Owner 山东绅联药业股份有限公司
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap