Category: 20265-97-8

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 20265-97-8, name is 4-Methoxyaniline hydrochloride, A new synthetic method of this compound is introduced below., SDS of cas: 20265-97-8

6-Methoxy-3-nitroquinoline 14. p-Anisidine hydrochloride (35.0 g, 219.4 mmol) was weighed into a dry 300 mL three-necked round-bottomed flask, equipped with a magnetic stirring bar, a pressure-equalizing addition funnel, a solid addition funnel and a thermometer. Glacial acetic acid (150 mL) was added to the solid, with vigorous stirring to maintain a homogeneous suspension. To this suspension was added sodium nitromalonaldehyde monohydrate (12.0 g, 76.4 mmol) and the mixture stirred for 1.0 h at 25 C. A short-path distillation head was placed on the flask and approximately 120 mL of acetic acid/water removed under reduced pressure at 40 C. To the residue (imine 13) was added glacial acetic acid (40 mL) and sulfolane (75 mL). The resulting solution was flushed with argon to:remove air and the flask immersed in an oil bath preheated to 195 C. The mixture was vigorously stirred while acetic acid was removed by distillation. When the temperature reached 184-185 C. the mixture was stirred for a further 15 min at 185 C. and then poured (while still at ca. 180 C.) onto crushed ice (750 g). The resulting solution was allowed to stand in a refrigerator (overnight) until precipitation was complete. The dark brown solid precipitate was filtered and transferred to a round-bottomed flask (500 mL) containing 2M hydrochloric acid (250 mL). The mixture was heated at reflux for 50-60 min and the boiling; solution filtered through a preheated Buchner funnel to remove an insoluble brown gum. The hot filtrate was cooled to ca. 4 C. and extracted with chloroform (4*50 mL). The combined extracts were dried (MgSO4) and the chloroform removed on a rotatory evaporator to give the crude 3-nitro-6-methoxyquinoline 14 (9.3 g, brown solid).

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference:
Patent; Board of Regents, The University of Texas System; US5442065; (1995); A;,
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Application of 20265-97-8, 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. 20265-97-8, name is 4-Methoxyaniline hydrochloride belongs to ethers-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

General procedure: 4-methyl-4?-hydroxyazobenzene (Azo1). 6,8 g (0.05 mol) as hydrochloride was dissolvedin 100 mL hydrochloric acid (2M). Solution was cooled by ice bath up to0C and solution of 3,3 g (0.05 mol) sodium nitrite in minimal volume of water wasadded slowly. To the cooled solution of phenol 4,4 g (0.05 mol) in water the diazoniumsalt was added under stirring. Yellow azodye precipitate was filtered, washedby cooled water and dried. Substance purification was made by recrystallization fromisopropanol.

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

Reference:
Article; Tarasenko, Vitaliy; Nadtoka, Oksana; Syromyatnikov, Vladimir; Molecular Crystals and Liquid Crystals; vol. 590; 1; (2014); p. 97 – 104;,
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20265-97-8, name is 4-Methoxyaniline hydrochloride, belongs to ethers-buliding-blocks compound, is considered to be a conventional heterocyclic compound, which is widely used in drug synthesis. The chemical synthesis route is as follows. category: ethers-buliding-blocks

General procedure: A cold solution of aryldiazonium salt (2.0 mmol) was preparedby adding a solution of NaNO2 (2.2 mmol, 0.15 g into 1.0 mL H2O) toa cold solution of arylamine hydrochloride (2.0 mmol of arylaminein 1.5 mL conc. HCl). The resulting solution of aryl diazonium saltwas added drop wise to a mixture of compound (II) (2.0 mmol,0.43 g) in water (15 mL) containing NaOH (25 mmol, 1.0 g) at0e5 C. The pH of the reaction mixture was maintained at 9e10 byadding 2.5% sodium hydroxide solution. Then, the reaction mixturewas stirred for 2 h at the same temperature and the precipitate wasfiltered off and the resulting solid was washed with cold ethanoland dried at 50 C in an oven. The crude product was purified usingthe recrystallization method as mentioned in Table 1. Under thesame reaction conditions, a series substituted arylazo quinolonedyes were obtained in satisfactory yields (Table 1, Scheme 2).

The synthetic route of 20265-97-8 has been constantly updated, and we look forward to future research findings.

Reference:
Article; Rufchahi, E.O. Moradi; Gilani, A. Ghanadzadeh; Taghvaei; Karimi; Ramezanzade; Journal of Molecular Structure; vol. 1108; (2016); p. 623 – 630;,
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Related Products of 20265-97-8, 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. 20265-97-8, name is 4-Methoxyaniline hydrochloride belongs to ethers-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

N-Acetyl-p-anisidine (3u).[17] p-Anisidine hydrochloride (0.80 g, 0.0050 mol) and trimethyl orthoacetate (0.66 g, 0.0055 mol were combined in a 10 mL round bottomed flask and heated under gentle reflux while being stirred for 1 hours. The homogeneous solution was then evaporated under reduced pressure to yield crude product that was crystallized from H2O/EtOH affording colorless plates (78%).

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, 4-Methoxyaniline hydrochloride, other downstream synthetic routes, hurry up and to see.

Reference:
Article; Di Grandi, Martin J.; Bennett, Caitlin; Cagino, Kristen; Muccini, Arnold; Suraci, Corey; Saba, Shahrokh; Synthetic Communications; vol. 45; 22; (2015); p. 2601 – 2607;,
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Synthetic Route of 20265-97-8, A common heterocyclic compound, 20265-97-8, name is 4-Methoxyaniline hydrochloride, molecular formula is C7H10ClNO, its 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.

A solution of 2-oxazolidinone (1.5 g, 17.2 mmol) in 2-(2-ethoxyethoxy)ethanol (20 mL) was treated with p-anisidine hydrochloride (2.1 g, 17.2 mmol) and heated in the microwave at 150 C. at 300 W for 10 min. The solution was cooled to rt and Et2O (50 mL) was added. The resulting solid precipitate was filtered and washed with Et2O (3¡Á20 mL). HPLC: Rt=0.23. MS (ESI): mass calcd. for C9H14N2O, 166.1; m/z found, 150 [M-16]+.

The synthetic route of 20265-97-8 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Allen, Darin; Choong, Ingrid; Lew, Willard; US2008/207683; (2008); A1;,
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

20265-97-8, These common heterocyclic compound, 20265-97-8, name is 4-Methoxyaniline hydrochloride, its 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.

p-anisidine hydrochloride (0.01 mol) was dissolved in a solution of concentrated hydrochloric acid (0.02 mol) in 50 ml of water. The mixture was cooled to 273 K on an ice water bath, and then sodium nitrite (0.015 mol) was dissolved in a small amount of water and added dropwise with vigorous stirring. The reaction mixture was stirred for1h, and then ethylenediamine dihydrochloride (0.0025 mol) was added. After the intense stirring for 10 min, KOH (0.04 mol) in 100 ml of water was added dropwise.The reaction took place immediately, and, as a result, the solution changed its color.The precipitate was collected by the vacuum filtration and dried at room temperature in vacuum. Yield 80%.1H-NMR (400 MHz, DMSO-D6, d, ppm) 7.50 (d, 8H, Ar), 6.90 (d, 8H, Ar), 3.84 (s,12H, -CH3), 3.1 (s, 4H, -CH2-) IR (KBr): 3000, 2934, 1602, 1504, 1448, 1248, 1028, 834

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of 20265-97-8.

Reference:
Article; Vyshnevsky, Dmitry; Syromyatnikov, Vladimir; Kolendo, Alexey; Molecular Crystals and Liquid Crystals; vol. 672; 1; (2018); p. 73 – 80;,
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

20265-97-8, A common heterocyclic compound, 20265-97-8, name is 4-Methoxyaniline hydrochloride, molecular formula is C7H10ClNO, its 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.

General procedure: Three stock solutions were prepared and connected to the flow reactor feed lines for Pumps A-C (see Figure 3 for a pictorial layout). Pump A delivered hydrochloric acid (0.84 M), Pump B a solution of aqueous sodium nitrite (0.98 M) and pump C delivered an aqueous solution of ascorbic acid (0.35 M). In addition a further pump was used to provide the solutions of aniline as their HCl salts dissolved in water (0.35 M). The entire reactor was maintained under positive internal pressure using a 75 psi back pressure regulator at the exit of the reactor. To initiate the reaction each flow channel was pumped at 0.5 mL/min. Progressing through the reactor; Channel A and B were mixed in a Uniqsis mixer chip of 0.27 mL internal volume (16 s residence time) before passing into a 2.75 mL PFA tubular residence coil (165 s residence time). The combined flow was then further united with the aniline solution mixing in a second Uniqsis mixer chip of 2 mL internal volume (80 s residence time). The reacting solution then passed into a 5 mL residence PFA foil coil (150 s residence time, the solution turns pale yellow to orange). The whole initial stage mixing unit was temperature regulated (10 C) using a Polar Bear Plus flow reactor unit. In the second stage reactor the freshly prepared diazonium mixture (combined flow rate 2 mL/min) was united at an Upchurch peek T-mixer with a solution of ascorbic acid delivered from Pump C set at 0.5 mL/min. The flow stream was then progressed into a 52 mL PFA flow coil (20.8 min residence time).The isolation of certain intermediate hydroxamic esters, namely 13-18, could be achieved by immediate extraction of the reactor output with ethyl acetate (5 volumes) and washing the organic phase with sodium hydrogen carbonate (2 M; 2). The organic solution was dried over MgSO4, filtered and concentrated in vacuo to provide a pale yellow solid which was triturated with a 1:1 mixture of hexane and acetone to furnishing the desired product. Alternatively, the output solution was collected and left to stir for 1 h to ensure complete hydrolysis to the corresponding oxamic acid, 1-12, had occurred. The products were isolated by basification of the reaction mixture pH ~9 followed by extraction with EtOAc (3 volumes). The aqueous solution was then acidified to pH ~4 and extracted with EtOAc (3 volumes), the organic phase was dried over MgSO4, the solvent evaporated to yield compounds 1-12. Note: for compounds 1-12 a proton signal sites under the residual DMSO signal.

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

Reference:
Article; Hu, Te; Baxendale, Ian R.; Baumann, Marcus; Molecules; vol. 21; 7; (2016);,
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20265-97-8, The chemical industry reduces the impact on the environment during synthesis 20265-97-8, name is 4-Methoxyaniline hydrochloride, I believe this compound will play a more active role in future production and life.

p-Anisidine hydrochloride (23.14 g, 132.5 mmol) was dissolved in ethanol (400 mL) and TRIFLUOROACETALDEHYDE ethyl hemiacetal (20 mL, 172.3 mmol) was added and refluxed overnight. The reaction was concentrated, and the crude compound was redissolved in N, N-dimethylformamide (150 mL) and cooled to 0C. N-BROMOSUCCINIMIDE (23.59 g, 132.5 mmol) was added to the solution over five minutes. The reaction was warmed to rt and stirred overnight. The reaction was quenched with water (1000 mL) and ethyl acetate (5000 mL), extracted with ethyl ACETATE (3X500 ML), WASHED WITH brine (1×500 ML) 7 DRIED OVER NA2804, concentrated, and purified by flash chromatography using 0-10% ethyl acetate/hexanes as eluent afforded 18. 8 g (48%) of the hydrazone intermediate

The chemical industry reduces the impact on the environment during synthesis 4-Methoxyaniline hydrochloride. I believe this compound will play a more active role in future production and life.

Reference:
Patent; BRYSTOL-MYERS SQUIBB COMPANY; WO2004/83177; (2004); A2;,
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem