Category: 2635-13-4

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. Formula: C7H5BrO2, 2635-13-4, Name is 5-Bromobenzo[d][1,3]dioxole, SMILES is BrC1=CC=C(OCO2)C2=C1, in an article , author is Requejo, Patricia F., once mentioned of 2635-13-4.

Study of Liquid-Liquid Equilibrium of Aqueous Two-Phase Systems Based on Ethyl Lactate and Partitioning of Rutin and Quercetin

Two ethyl lactate (EL)-based aqueous two-phase systems (ATPSs) were studied at T = 298.15 K and atmospheric pressure. Sodium tartrate and potassium sodium tartrate organic salts have been used to form biphasic systems. To assess the phase splitting, binodal curves and tie-lines were obtained experimentally by the cloud point method and a technique, which consist of the density and refractive index, respectively. Binodal curves were fitted with the Merchuk equation obtaining a good fit. Moreover, modeling with the universal quasichemical thermodynamic equation was carried out to accurately represent the two-biphasic systems. Furthermore, experimental binodal curves obtained in this work and literature results for the same systems and for systems with EL and other salts were analyzed regarding their similarity. Finally, the application of the adopted ATPS in the partitioning of two flavonoids, rutin and quercetin, was studied in terms of the partition coefficients and the percentage of extraction. Rutin and quercetin showed better affinity to the EL-rich phase, evidencing that the use of the proposed ATPS may be a successful technique in the biotechnological industry for the separation of each flavonoid.

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 2635-13-4, you can contact me at any time and look forward to more communication. Formula: C7H5BrO2.

Electric Literature of 2635-13-4, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 2635-13-4, Name is 5-Bromobenzo[d][1,3]dioxole, SMILES is BrC1=CC=C(OCO2)C2=C1, belongs to bromides-buliding-blocks compound. In a article, author is Pelliccioli, Valentina, introduce new discover of the category.

Diversified Syntheses of Tetrathia[7]helicenes by Metal-Catalyzed Cross-Coupling Reactions

Efficient and versatile synthetic routes to functionalized tetrathia[7]helicenes (7-THs) are described. The key intermediates of these methodologies are 2-bromo-3,3 ‘-bibenzo[1,2-b:4,3-b ‘]dithiophenes (1), synthesized through a palladium-catalyzed homocoupling reaction between two benzo[1,2-b:4,3-b ‘]dithiophene units followed by a regioselective alpha-bromination. Direct palladium-catalyzed annulation of bromides 1 with internal alkynes provides a set of 7,8-disubstituted 7-THs 2 in moderate to good yields (46-80 %). Otherwise, 7-monosubstituted 7-THs 4 have been prepared through Sonogashira coupling of 1 with terminal alkynes, followed by platinum- or indium-promoted cycloisomerization of alkynyl intermediates 6. Finally, the versatility of bromides 1 has also been demonstrated by using them for the preparation of benzo (hetero) fused 7-TH derivatives 7 via Suzuki coupling with (hetero)arylboronic acids and the photocyclization of the obtained intermediates 9.

Electric Literature of 2635-13-4, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 2635-13-4.

Application of 2635-13-4,Some common heterocyclic compound, 2635-13-4, name is 5-Bromobenzo[d][1,3]dioxole, molecular formula is C7H5BrO2, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

To a screw cap vial were added Pd(PPh3)2Cl2 (58.3 mg, 81.4 mumol), CuI (31.6 mg, 163 mumol),anhydrous DMF (0.33 mL), 4-bromo-1,2-(methylenedioxy)benzene (10d) (200 muL, 1.63 mmol)and Et3N (2.28 mL, 16.4 mmol) at rt. The solution was bubbled with argon gas for 5 min toremove the dissolved gases. Then, trimethylsilylethyne (350 muL, 2.44 mmol) was added, andthe reaction mixture was stirred at 90 C for 24 h. Upon completion of the reaction, the reaction mixture was concentrated by rotary evaporation. Purification by column chromatography(hexanes) yielded 11d (153 mg, 43%) as a brown liquid.

The synthetic route of 2635-13-4 has been constantly updated, and we look forward to future research findings.

Reference:
Article; Jeong, Yunkyung; Lee, Jooyeon; Ryu, Jae-Sang; Bioorganic and Medicinal Chemistry; vol. 24; 9; (2016); p. 2114 – 2124;,
Bromide – Wikipedia,
bromide – Wiktionary

Adding a certain compound to certain chemical reactions, such as: 2635-13-4, name is 5-Bromobenzo[d][1,3]dioxole, belongs to bromides-buliding-blocks compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 2635-13-4, Product Details of 2635-13-4

Step 1a. 5-Bromo-6-iodobenzo[d][1,3]dioxole (Compound 0102-1) A solution of 5-bromobenzo[d][1,3]dioxole (10.0 g, 50.0 mmol), anhydrous acetonitrile (150 mL), TFA (11.4 g, 100.0 mmol) and NIS (33.7 g, 150.0 mmol) was stirred at room temperature for 24 h. The solvent was removed under reduce pressure and the crude purified by column chromatography on silica gel (petroleum) to yield the title compound 0107-1 as a white solid (18.5 g, 91%): 1H NMR (DMSO-d6) delta 5.99 (s, 2H), 7.10 (s, 1H), 7.26 (s, 1H).

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 5-Bromobenzo[d][1,3]dioxole, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Cai, Xiong; Qian, Changgeng; US2010/184801; (2010); A1;,
Bromide – Wikipedia,
bromide – Wiktionary

Application of 2635-13-4, In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 2635-13-4 as follows.

201mg (1mmol) of 3,4-methylenedioxybromobenzene, 1mL aqueous ammonia (25-28%, 13.3mmol), 8mg (0.1mmol) CuO, 79mg (0.2mmol) diethylenetriaminepentaacetic acid, 112mg ( 2mmol) KOH, 1mL H2O was added 10mL reaction tube, sealed and reacted at 100C for 12h. After the reaction was stopped, extraction with ethyl acetate, washed with brine, dried over anhydrous sodium sulfate, filtered, and the filtrate was evaporated under reduced pressure, purified by silica gel column chromatography purification, in 3,4-methylenedioxyaniline 100mg, The yield was 73%.

According to the analysis of related databases, 2635-13-4, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Sun Yat-Sen University; ZHU, XIN HAI; YANG, BO; LIAO, LI HAO; CENG, YONG HENG; WAN, YI QIAN; (9 pag.)CN103739417; (2016); B;,
Bromide – Wikipedia,
bromide – Wiktionary

Application of 2635-13-4,Some common heterocyclic compound, 2635-13-4, name is 5-Bromobenzo[d][1,3]dioxole, molecular formula is C7H5BrO2, traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

EXAMPLE 3 Alternative syntheses of (S)-alpha-methyl-1,3 benzodioxole-5-ethanol 3.47 grams of 4-bromo-1,2(methylenedioxy)benzene were dissolved in 100 ml of tetrahydrofuran at -78 C., 13.9 ml of 1.3M sec-butyllithium in cyclohexane was then added to consume the aryl halide in less than 30 minutes. 1.00 grams of (S)-(-)-propylene oxide in 2 ml THF was added by syringe and the solution stirred for 45 minutes. The solution was then warmed to 23 C. for 16 hours. The reaction mixture was poured into 3M ammonium chloride solution and the product isolated by extraction with ethyl acetate. The combined extracts were dried over magnesium sulfate filtered through florisil and concentrated by rotary evaporation. The residual oil was purified by silica gel chromatography and eluted with a 50:50 mixture of hexane and diethyl ether to yield 1.40 g (45%) of the subtitled intermediate. Pchem: [alpha]365 +117.2 (c 1.0, CHCl3) TLC Rf =0.26 (50:50 hexane:ether); IR (CHCl3) 3598, 3012, 2973, 2887, 1490, 1249, 1041 cm-1; 13 C NMR (CDCl3) d 147.75, 146.19, 132.26, 122.27, 109.68, 108.30; mass spectrum, m/z (FD, M+) 180; Anal. Calcd. for C10 H12 O3: C, 66.65; H, 6.71. Found: C, 66.42; H, 6.66.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 5-Bromobenzo[d][1,3]dioxole, its application will become more common.

Reference:
Patent; Eli Lilly and Company; US5795886; (1998); A;,
Bromide – Wikipedia,
bromide – Wiktionary

In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 2635-13-4 as follows. Application In Synthesis of 5-Bromobenzo[d][1,3]dioxole

General procedure: A 10-mL vial was charged with aryl halide (0.5 mmol), Cs2CO3 (1 mmol), Cu2O (0.05 mmol), N-containing heterocycles (0.75 mmol), DMF (1 mL), and a magnetic stir bar. The mixture was stirred at 120 C (130 C for entry 19). The reaction mixture was held at this temperature for 12 h (24 h for entry 18, 20, 21, and 25). After allowing the mixture to cool to room temperature, the reaction mixture was extracted with ethyl acetate (3 10 mL), dried over anhydrous Na2SO4, and concentrated in vacuo. The residue was purified by silica gel chromatography (ethyl acetate/petroleum ether as the eluent) to provide the target products 3a-3t.

According to the analysis of related databases, 2635-13-4, the application of this compound in the production field has become more and more popular.

Reference:
Article; Wang, Xiaochuang; Wang, Meiji; Xie, Jianwei; Synthetic Communications; vol. 47; 19; (2017); p. 1797 – 1803;,
Bromide – Wikipedia,
bromide – Wiktionary

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 2635-13-4, name is 5-Bromobenzo[d][1,3]dioxole belongs to bromides-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below. 2635-13-4

Benzo[1,3]dioxole-5-carbaldehyde (1.80 g, 11.96 mmol), 5-bromobenzo[1,3]dioxole (2.65 g, 13.16 mmol), and n-butyl lithium (5.26 ml, 13.16 mmol) were treated in the same manner as described above for the synthesis of (2,3-dihydrobenzo[1,4]dioxin-6-yl)-(3,5-dimethoxyphenyl)methanol. The crude material was purified via flash column chromatography (5% EtOAc in hexane gradient to 40% EtOAc in hexane in about 40 min.) to give bis-benzo[1,3]dioxol-5-yl-methanol as a light brown oil (2.69 g, 83%): 1H-NMR (CDCl3) 6.86-6.74 (m, 6H, Ar), 5.93 (s, 4H, 2CH2), 5.68 (d, J=3 Hz, 1H, CHOH), 2.16 (d, J=3 Hz, 1H, OH). The product was carried over to the next step.

The synthetic route of 2635-13-4 has been constantly updated, and we look forward to future research findings.

Reference:
Bromide – Wikipedia,
bromide – Wiktionary