1,2,3,4-Tetrahydronaphthalene compound and preparation method and application thereof

A compound, tetrahydronaphthalene technology, applied in the field of organic compound synthesis, can solve the problems of harsh preparation conditions, limited application scope, unfriendly environment, etc., and achieve the effect of simplifying operation, broadening application scope and widening scope.

Active Publication Date: 2018-11-13
PEKING UNIV SHENZHEN GRADUATE SCHOOL
View PDF4 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The invention provides a 1,2,3,4-tetrahydronaphthalene compound and a preparation method thereof to solve the problem of harsh preparation conditions, low yield and complex process of existing 1,2,3,4-tetrahydronaphthalene compounds. Technical problems such as unfriendly environment and limited application range

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
  • 1,2,3,4-Tetrahydronaphthalene compound and preparation method and application thereof
  • 1,2,3,4-Tetrahydronaphthalene compound and preparation method and application thereof
  • 1,2,3,4-Tetrahydronaphthalene compound and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0097] In one embodiment, the preparation method of the 1,2,3,4-tetrahydronaphthalene compound comprises the following steps:

[0098] S01: respectively provide the styrene compound A and the olefin compound B represented by the following structural formula:

[0099]

[0100] S02: Add the styrene compound A and the olefin compound B into a reaction system containing a visible light catalyst, a co-catalyst and a solvent to react at a temperature of -80-100°C to obtain the following structure represented by (I) The 1,2,3,4-tetrahydronaphthalene compounds shown,

[0101]

[0102]Specifically, in the above step S01, R in the molecular structural formula of styrene compound A 1 , R 2 , R 5 , R 6 , R 7 , R 8 The represented group is as above in the invention embodiment 1,2,3,4-tetrahydronaphthalene compound molecular structure general formula (I) in R 1 , R 2 , R 5 , R 6 , R 7 , R 8 The groups represented are the same.

[0103] R in the molecular structure formula...

Embodiment 1

[0136] Example 1 provides 1-(4-methoxyphenyl)-4-methyl-1,2,3,4-tetrahydronaphthalene and its preparation method.

[0137] The structural formula of the 1-(4-methoxyphenyl)-4-methyl-1,2,3,4-tetrahydronaphthalene is shown in the following molecular structural formula I1:

[0138]

[0139] Its preparation steps are as follows:

[0140] In a dry 10 mL test tube, add mesitylene-substituted acridinium salt visible light catalyst (0.01 mmol, 0.1 eq), diphenyl disulfide co-catalyst (0.01 mmol, 0.1 eq) and 2 mL of anhydrous dichloroethane, argon Replace three times, add 0.3mmola-methylstyrene, replace with argon three times again, seal the reaction test tube and stir at room temperature for 10 min. Dissolve p-methoxystyrene benzene (0.1mmol, 1.0eq) in 2mL of anhydrous dichloroethane, and slowly add it into the reaction system, while adding it, irradiate it with two blue LEDs with a power of 15w, add and react The time is 10h. After the reaction was completed, the filtrate was spi...

Embodiment 2

[0143] Example 2 provides 1-(4-methoxyphenyl)-4-ethyl-1,2,3,4-tetrahydronaphthalene and its preparation method. The structural formula of the 1-(4-methoxyphenyl)-4-ethyl-1,2,3,4-tetrahydronaphthalene is shown in molecular structural formula I2 below:

[0144]

[0145] Its preparation method refers to the preparation method of 1-(4-methoxyphenyl)-4-methyl-1,2,3,4-tetrahydronaphthalene in Example 1, the difference is that a-ethylstyrene (0.3mmol) instead of a-methylstyrene, the filtrate was spin-dried, and separated by column chromatography to obtain the target product as a colorless oily liquid with a yield of 77% and a dr value of 1:1.

[0146] The product I2 prepared is subjected to characterization data analysis, and the result is: 1 HNMR (300MHz, Chloroform-d) δ7.29(td, J=8.5, 1.5Hz, 1H), 7.19(tt, J=7.8, 2.1Hz, 1H), 7.12–6.98(m, 3H), 6.87(qd ,J=5.8,5.2,2.0Hz,3H), 4.09(t,J=11.1,7.0Hz,1H),3.82(s,3H),2.83(ddq,J=19.4,9.8,5.3Hz,1H), 2.24(dddd,J=12.6,8.7,5.6,2.8Hz,1H),2.10–...

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 1,2,3,4-tetrahydronaphthalene compound and a preparation method and application thereof. The 1,2,3,4-tetrahydronaphthalene compound has a molecular structural formula shown asformula (I) that is shown in the description. The preparation method of the 1,2,3,4-tetrahydronaphthalene compound comprises steps, such as subjecting styrene compound A, olefine compound B, a visiblelight catalyst, a cocatalyst and a solvent to reacting. The 1,2,3,4-tetrahydronaphthalene compound has a tetrahydronaphthalene basic framework containing electron-withdrawing group and electron-donating group substations, and is widely applicable to the preparation of functional materials and the synthesis of pharmaceutical intermediates, especially polycyclic-structure compounds. The preparationmethod herein is simple and has low reaction condition requirements, the reaction process has good safety and controllability, atom utilization rate and production efficiency are high, regio-and stereo-selectivity of products is effectively ensured, and the products have no pollution.

Description

technical field [0001] The invention belongs to the technical field of organic compound synthesis, and specifically relates to a 1,2,3,4-tetrahydronaphthalene compound and a preparation method and application thereof. Background technique [0002] Polycyclic compounds refer to a class of compounds that contain multiple ring units in their molecular structure. Polycyclic compounds are not only extremely important pharmaceutical fragments and intermediates, but also potential biologically active molecules. Starting from polycyclic products and modifying them with known chemical means is an important part of the research and development of new drug molecules. [0003] Among them, 1,2,3,4-tetrahydronaphthalene compounds are important ones among polycyclic compounds. 1,2,3,4-Tetrahydronaphthalene compounds are important building blocks for the synthesis of pharmaceutical intermediates, especially heterocyclic compounds and the preparation of functional materials. The classic m...

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): C07C41/30C07C43/21C07C43/225C07C17/275C07C25/22
CPCC07C17/275C07C25/22C07C41/30C07C43/21C07C43/225
Inventor 黄湧王雷锋陈杰安
Owner PEKING UNIV SHENZHEN GRADUATE SCHOOL
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