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A kind of thioxanthone carboxylate photoinitiator and preparation method thereof

A technology of thioxanthone carboxylate and thioxanthone formyloxymethyl propionate, which is applied in organic chemistry and other fields, can solve the problems of low volatility, large synthesis pollution, and high cost, and achieve mild reaction conditions and simple operation , low cost effect

Active Publication Date: 2018-01-02
TIANJIN JIURI NEW MATERIALS CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Under the increasing sensitivity to the pollution of foreign compounds in food and pharmaceutical packaging and the increasingly stringent environmental protection pressure, it is difficult for the currently commercially available thioxanthone photoinitiators to meet the above requirements, which have high activity, good compatibility, Macromolecular thioxanthone photoinitiators with low extraction, low migration and low volatility will gradually be recognized by the market
[0006] Patent CN101230056 discloses a class of macromolecular thioxanthone initiators, but the disadvantage is that the synthetic pollution of phenolic hydroxythioxanthone is relatively large, the waste water is difficult to treat, and the cost is high, which restricts the application of this type of photoinitiator
WO2003033492 discloses that 2-hydroxythioxanthone and various polyethers are used as raw materials to prepare multifunctional thioxanthone photoinitiated derivatives, but there is also the problem of large pollution in the synthesis of 2-hydroxythioxanthone
US200400559133 has improved the raw material synthesis process in the above-mentioned patents, eliminating the pollution of phenol, but the post-treatment of a large amount of concentrated sulfuric acid is also very difficult
US6025408 and US4594400 disclose the polymerizable monomer derived from thioxanthone carboxylic acid, and copolymerize with other monomers to obtain a macromolecular photoinitiator connected with thioxanthone ester derivatives in the polymerization side chain, but in In practical application, because of its high viscosity, there are great problems in the application process
[0007] CN200410093977.9 discloses that a class of thioxanthone-2-carboxylic acid derivatives exhibits low volatility, low extraction, and low migration characteristics, but the cost of raw materials for preparing such compounds is high, and their photoinitiating activity is slightly lower than that of thioxanthone-2-carboxylic acid derivatives. 4-Carboxylic acid derivatives, the practical application is limited
CN201010218422.8 discloses thioxanthone-4-carboxylic acid polyethylene glycol-200-diester, thioxanthone-4-carboxylic acid polyethylene glycol-300-diester, thioxanthone-4-carboxylic acid poly Tetrahydrofuran-250-diester has the characteristics of high activity, low volatility, low extraction, and low migration, but the melting point of this type of compound is not high, it is not easy to store and transport, it is difficult to maintain the appearance at a slightly higher room temperature, and it cannot be continuously produced; the compatibility is not good. High, increasing the difficulty of purification, but also increasing the difficulty of industrial production
Simultaneously, the preparation method of these two types of thioxanthone derivatives cannot be carried out by the transesterification of general thioxanthone carboxylate (such as methyl ester or ethyl ester), resulting in severe transesterification reaction conditions and severe The reaction is not easy to complete, making it difficult to scale up production on a large scale

Method used

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  • A kind of thioxanthone carboxylate photoinitiator and preparation method thereof
  • A kind of thioxanthone carboxylate photoinitiator and preparation method thereof
  • A kind of thioxanthone carboxylate photoinitiator and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0049] Example 1: Methyl 2-(thioxanthone-4-formyloxy)propionate

[0050] In a 250ml four-neck flask equipped with mechanical stirring, add 25.0g thioxanthone-4-formyl chloride, 125ml chlorobenzene, 11.1g triethylamine, 10.4g methyl lactate, heat to 60~70℃, reaction 5. After hours, suction filtration, the filtrate was cooled to 5~10℃, stirred and crystallized for 2 hours, and then filtered to obtain a crude product. The crude product was recrystallized from chlorobenzene. After drying, 27.5g of pale yellow flake crystals were obtained. The yield was 88%, and the content was ≥98.5%. . 1 H NMR (DMSO) δ: 8.82 (m, 1H), 8.56 (m, 1H), 8.43 (m, 1H), 7.90(d, 1H), 7.75 (m, 2H), 7.61 (m, 1H), 5.37 (m, 1H), 3.76 (s, 3H), 1.62 (d, 3H).

Embodiment 2

[0051] Example 2: Methyl 2-(thioxanthone-4-formyloxy)propionate

[0052] In a 250ml four-neck flask equipped with mechanical stirring, add 25.0g thioxanthone-4-formyl chloride, 125ml chlorobenzene, 17.6g diisopropylethylamine, 18.9g methyl lactate, and heat to 80~90℃, React for 4 hours, filter with suction, cool the filtrate to 5~10℃, stir and crystallize for 2 hours, and then filter with suction to obtain a crude product. The crude product is recrystallized with chlorobenzene. After drying, 28.3g of yellow flake crystals are obtained. The yield is 91%, and the content is ≥98.5. %.

Embodiment 3

[0053] Example 3: Methyl 2-(thioxanthone-2-formyloxy)propionate

[0054] In a 250ml four-necked flask equipped with mechanical stirring, add 25.0g thioxanthone-2-formyl chloride, 125ml chlorobenzene, 11.1g triethylamine, 10.4g methyl lactate, heat to 60~70℃, reaction 5. After hours, suction filtration, the filtrate was cooled to 5~10℃, stirred and crystallized for 2 hours, and then filtered to obtain a crude product. The crude product was recrystallized from chlorobenzene. After drying, 29.0g of pale yellow flake crystals were obtained. The yield was 93% and the content was ≥98.5%. . 1 H NMR (DMSO) δ: 8.45 (d, 1H), 8.14 (m, 1H), 7.99 (m, 1H), 7.83(d, 1H), 7.62 (m, 2H), 7.42 (m, 1H), 5.53 (m, 1H), 3.88 (s, 3H), 1.55 (d, 3H).

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Abstract

The invention discloses a new thioxanthone carboxylic ester photoinitiator and a preparation method thereof. The invention relates to a preparation method of thioxanthone carboxylic ester. The thioxanthone carboxylic ester is a compound with the structure of a formula (I) as shown in the specification, wherein the carboxylic ester substituent group of the thioxanthone is at position 2 and position 4; each R1 is independently selected from hydrogen, halogen, C1-C12 alkyl, C3-C6 naphthenic base and C1-C12 alkoxy; each of R2 and R3 is independently selected from hydrogen, halogen, C1-C18 alkyl, C3-C6 naphthenic base and C1-C18 alkoxy; X is independently selected from multi-hydroxyl micromolecular compound (wherein the hydroxyl number is 2-6) and C1-C18 alkoxy; and m is 1-6. The preparation method overcomes the defect that the generally used thioxanthone carboxylic ester has low ester exchange activity by introducing a methyl lactate group and improving the condition of ester exchange reaction; the reaction condition is mild and ester exchange can be finished in a short time; and the preparation method is suitable for industrialized production.

Description

Technical field [0001] The content of the present invention is a new thioxanthone carboxylate photoinitiator and a preparation method of the photoinitiator. Background technique [0002] UV light curing technology is an environmentally friendly technology in the fields of coatings, inks, adhesives, etc. The main body of the material is generally composed of acryl resin, polyol acrylate and photoinitiator, and it is fully cured under the action of sufficient ultraviolet light. Compared with the traditional solvent-containing system, it has outstanding characteristics such as no solvent emission, high efficiency and energy saving, so it is used in many fields. With the increasing application of UV light curing materials, some unexpected problems have appeared, such as the problem of baby milk incident in 2005. During sampling inspection of a batch of baby milk, it was found that the printing of this batch of milk packaging materials contained a A chemical substance called isopropy...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07D335/16C08F2/46C08G59/17
CPCC07D335/16C08F2/46C08G59/1416
Inventor 赵建新董子瑞董月国罗想杨天艳毛桂红武瑞张齐赵国锋
Owner TIANJIN JIURI NEW MATERIALS CO LTD
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