A method for synthesizing 3,6-dibromo-9-bromophenyl-9h-carbazole

A technology of phenylcarbazole and a synthesis method, applied in the field of chemistry, can solve problems such as aggravating the difficulty of purification, low total yield, and increase reaction cost, avoid coupling process and metal residues, facilitate industrialized production of enterprises, reduce The effect of the discharge of the three wastes

Active Publication Date: 2021-10-29
SINOSTEEL NANJING NEW MATERIALS RES INST CO LTD
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] Among the above-mentioned synthetic routes, the reaction of route I has a low yield and requires the use of pre-modified carbazole bromide, which increases the cost of the route; Environmental challenges; the third is that it needs to be reacted at high temperature (150°C) for a long time (24h), which may lead to dark color of the reaction solution and increase the difficulty of later purification
[0009] The route II one needs to use expensive p-bromoiodobenzene as the aryl source, which increases the reaction cost and is unfavorable for industrialized production; the second is to use N-bromosuccinimide (NBS) as the bromine source, which has poor atom economy, The by-product of succinimide will be produced, which increases the difficulty and cost of purification in the later stage; the third is that this reaction requires a two-step method, and the total yield is low, which makes the route economically poor
[0010] For another example, in 2012, "Heilongjiang Science" 2012, Volume 3, Phase 1, Page 26-27, Li Meng et al published an article entitled "Synthesis of 3-bromo-9-phenylcarbazole", which Describes the one-step preparation of monobrominated or dibrominated compounds using N-phenylcarbazole and brominating reagents as raw materials. However, using NBS as a bromine source will generate butanediimine as a by-product after bromination, and the product Coexistence increases the treatment cost of the three wastes; in addition, this system requires the use of mixed solvents, which increases the difficulty of subsequent solvent recovery and further increases the process cost
Due to the chemical identity of the 3 and 6 positions of carbazole, the excess bromine source can simultaneously brominate the 3 and 6 positions to obtain dibrominated products, but for the weak electrophilicity of the N-phenyl para position, the bromine produced by NBS dissociation Positive ions are difficult to further efficiently add to it to complete the bromination process

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
  • A method for synthesizing 3,6-dibromo-9-bromophenyl-9h-carbazole
  • A method for synthesizing 3,6-dibromo-9-bromophenyl-9h-carbazole
  • A method for synthesizing 3,6-dibromo-9-bromophenyl-9h-carbazole

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0045]At room temperature, add 243.3g N-phenylcarbazole (99%, 1mol), 450mL DCM, 667.5g HBr (40%, 3.3mol), rotating speed 550rpm, 374.0g hydrogen peroxide (30%, 3.3 mol) was added dropwise through a constant pressure titration funnel, the rate of addition was 2mL / min, the drop was completed, and the reaction was carried out for 4 hours. Thin-layer chromatography (TLC) was used to monitor whether the reaction raw materials had reacted completely. The crude product was crystallized from ethyl acetate to obtain 406.26 g of tribromo-NPC with a content of 99.5% and a yield of 85.2%. The product was examined by NMR as figure 2 As shown in the figure: 1 H-NMR (400MHz, CDCl 3 ): δ8.19(s, 2H), 7.74(d, J=8.0Hz, 2H), 7.51(d, J=8.0Hz, 2H), 7.38(d, J=8.0Hz, 2H), 7.22(d , J=8.0Hz, 2H), mp=217-218°C. figure 1 It is the reaction equation of the synthesis reaction of this embodiment.

Embodiment 2

[0047] At room temperature, add 243.43g N-phenylcarbazole (99%, 1mol), 450mL DMF, 349.84g NaBr (99.9%, 3.4mol), rotating speed 550rpm, 385.33g hydrogen peroxide (30%, 3.4 mol) was added dropwise through a constant pressure titration funnel at a rate of 1mL / min. After the drop was completed, the reaction was carried out for 5 hours and monitored by thin-layer chromatography (TLC). Crystallization with ethyl acetate gave 344.28 g of tribromo-NPC with a content of 99.3% and a yield of 72.2%.

Embodiment 3

[0049] At room temperature, add 121.63g N-phenylcarbazole (99%, 0.5mol), 250mL DMF, 333.75g HBr (40%, 1.65mol) in 1L reaction flask, rotating speed 550rpm, 187.08g hydrogen peroxide (30%, 1.65mol) was added dropwise through a constant pressure titration funnel at a rate of 2mL / min. After the drop was completed, the reaction was carried out for 5 hours and monitored by thin-layer chromatography (TLC). After the reaction was completed, water and ethyl acetate were added for extraction, and the organic layer was precipitated to obtain a crude Crystallized with ethyl acetate to obtain 149.54 g of tribromo-NPC with a content of 99.6% and a yield of 62.3%. Because the present embodiment adopts polar solvent DMF, DMF has certain complexation with the positive bromide ion that in situ generates, has reduced the electrophilic ability of positive bromide ion, causes reaction yield low (solvent effect); Simultaneously bromine source Amount reduces to some extent compared with embodiment ...

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
quality scoreaaaaaaaaaa
Login to view more

Abstract

The invention discloses a method for synthesizing 3,6-dibromo-9-bromophenyl-9H-carbazole, belonging to the technical field of chemistry. The steps of the synthesis method are as follows: at room temperature, dissolve N-phenylcarbazole and bromination reagent in an organic solvent, stir and add an oxidizing agent, react for 4-8 hours, after the reaction, recover the solvent, extract, and the organic layer is desolvated, Recrystallization obtains 3,6-dibromo-9-bromophenyl-9H-carbazole, wherein the process of adding the oxidizing agent adopts a stepwise addition method or a titration method, while controlling the temperature of the reaction system to be lower than the boiling point of the organic solvent. The preparation method of the present invention adopts a one-step method at room temperature, using commercially available N-phenylcarbazole as a raw material, and under the action of brominating reagents and oxidants, tribromo-NPC can be obtained with high yield and high purity. , the method has mild and simple conditions, simple operation, low cost, high yield, and is easy for enterprises to produce industrially.

Description

technical field [0001] The invention relates to the technical field of chemistry, in particular to a method for synthesizing tribromo-N-phenylcarbazole by oxidative bromination of N-phenylcarbazole. Background technique [0002] Organic electrophosphorescent light-emitting devices (PhOLEDs), which are materials with a host-guest structure, have extremely high application potential in the fields of display and lighting. Carbazole has π-electron conjugated system, intramolecular electron transfer characteristics and lone pair electron heteroatoms, so carbazole and its derivatives have strong charge transport ability and photoelectric performance. A single carbazole molecule has poor photoelectric properties due to its weak conjugation system. Therefore, it is usually necessary to modify the carbazole site by bromination to realize the arylation / heteroarylation of the carbazole site, further expand the electronic conjugated system, and improve the charge transport ability. 3,...

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 Patents(China)
IPC IPC(8): C07D209/88
CPCC07D209/88
Inventor 吴忠凯裴晓东朱叶峰杨修光张玲申宝金骆艳华
Owner SINOSTEEL NANJING NEW MATERIALS RES INST CO LTD
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