Tag: M.W=100-200

Electric Literature of 6136-93-2, 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. 6136-93-2, name is 2,2-Diethoxyacetonitrile belongs to nitriles-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

EXAMPLE I Preparation of 2-Ethylidene-6-methyl-cis-3-heptenal A solution of 5.40 g of isobutylacetylene in 50 ml of diethyl ether is treated with 30 ml of 2.2 N n-butyllithium in hexane at -20 C, and after several minutes the resulting solution is treated with 8.50 g of diethoxyacetonitrile and then warmed slowly to room temperature. After about 1.5 hours the dark mixture is cooled and brought to a pH of about 2 with ten percent sulfuric acid. The layers are then separated and the organic layer is washed successively with water and saturated aqueous sodium bicarbonate solution and then dried over sodium sulfate. Evaporation of the solvent provides 4.6 g of a dark oil, shown by IR and NMR to contain 1,1-diethoxy-6-methyl-3-heptyn-2-one.

The synthetic route of 2,2-Diethoxyacetonitrile has been constantly updated, and we look forward to future research findings.

Reference:
Patent; International Flavors & Fragrances Inc.; US4024190; (1977); A;,
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Electric Literature of 1591-37-3, 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. 1591-37-3, name is 2-Amino-6-methoxybenzonitrile belongs to nitriles-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

EXAMPLE 46 9-Amino-8-methoxy-4-oxa-1,2,3,4-tetrahydroacridine Following the method of Example 7, but substituting 2-amino-6-methoxybenzonitrile for anthranilonitrile afforded the title compound (11%, m.p. 205-207 C.). 1 H-NMR (CDCl3, 300 MHz,delta): 2H, m, 7.33 ppm; 1H, dd, 6.57 ppm (J=3, 6 Hz); 2H, bs, 5.92 ppm; 2H, t, 4.29 ppm (J=2, 6 Hz); 3H, s, 3.95 ppm; 2H, t, 2.5 ppm (J=2, 6 Hz); 2H, m, 2.13-2.07 ppm; TLC: (90:10:1-methylene chloride:methanol:28% aqueous ammonia) Rf -0.49.

The synthetic route of 2-Amino-6-methoxybenzonitrile has been constantly updated, and we look forward to future research findings.

Reference:
Patent; Pfizer Inc.; US5202440; (1993); A;,
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Synthetic Route of 2042-37-7, 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 2042-37-7 as follows.

General procedure: The aryl halide (5.0 mmol), arylboronic acid (7.5 mmol), base (10.0 mmol), the calculated amount of thiourea, Pd and H2O (5 mL) were added to a flask containing a magnetic stir bar under air. The flask was sealed with a rubber septum and the contents were stirred at the specified temperature for the appropriate period of time. Upon completion, the reaction mixture was extracted using Et2O (3 10 mL). The solvent was removed on a rotary evaporator and the residue was purified by flash chromatography on silica gel to afford the desired product. The coupling products were characterized by 1H NMR and 13C NMR spectroscopy (see the Supporting Information). The identities of the products were confirmed by comparison with literature spectroscopic data.

According to the analysis of related databases, 2042-37-7, the application of this compound in the production field has become more and more popular.

Reference:
Article; Chen, Wei; Lu, Xiao-Yan; Xu, Bei-Hua; Yu, Wei-Guo; Zhou, Zi-Niu; Hu, Ying; Synthesis; vol. 50; 7; (2018); p. 1499 – 1510;,
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Reference of 6574-99-8, 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. 6574-99-8, name is 3,4-Dichlorobenzonitrile belongs to nitriles-buliding-blocks compound, it is a common compound, a new synthetic route is introduced below.

General Procedure C. The nitrile (10 mmol) was added in several portions, over 0.5 h to a solution of the nBuMgCl (12 mmol) in toluene (20 mL). The reactions were monitored by TLC and heated where necessary. Generally, after 2 h stirring at room temperature, the reaction was complete. The reaction mixture was poured onto ice and concentrated H2S04 (2 mL) was added. Hydrolysis of the intermediate imine usually occurred at room temperature after several minutes, however, for some substrates, heating was necessary to effect this transformation. The organics were extracted into Et20, dried (MgS04), filtered, and reduced to an oil in vacuo. Example 58 1-(3, 4-Dichloro-phenyl)-pentan-l-one. Following General Procedure C, this compound was prepared in 93% yield and employed in the next step of the reaction as the crude material.

The synthetic route of 3,4-Dichlorobenzonitrile has been constantly updated, and we look forward to future research findings.

Reference:
Patent; PRESIDENT AND FELLOWS OF HARVARD COLLEGE; ORGANIX, INC.; WO2005/34878; (2005); A2;,
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Adding a certain compound to certain chemical reactions, such as: 64248-62-0, name is 3,4-Difluorobenzonitrile, belongs to nitriles-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 64248-62-0, Application In Synthesis of 3,4-Difluorobenzonitrile

The reaction flask (250 mL) containing magnetic stirring bar was charged with 1,3,5-tris((trimethylsilyl)oxy)benzene (10.28 g, 30 mmol),followed by the addition of 3,4 -difluorobenzonitrile (13.90 g, 100 mmol). The reaction flask was purged with Argon, and anhydrous DMF (100mL) was added. Anhydrous cesium fluoride (1.52 g, 10 mmol) was carefully added in one portion, the reaction flask was capped with a septumconnected to a bubbler and stirred at 120 C for 24 hours. The reaction mixture was poured in water under vigorous stirring and the resultingprecipitate was filtered off and air dried. The title product was obtained after the re-crystallization from ethanol. The product was obtainedafter filtration as a white powder (9.2 g, 63 %).

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Reference:
Article; Chen, Hao; Cheng, Long; Dai, Sheng; Guo, Wei; Jiang, De-en; Jie, Kecheng; Jin, Wanqin; Liu, Gongping; Mahurin, Shannon Mark; Meyer, Harry M.; Popovs, Ilja; Wang, Song; Yang, Zhenzhen; Chem; vol. 6; 3; (2020); p. 631 – 645;,
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Application of 7357-70-2, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 7357-70-2, name is 2-Cyanothioacetamide, This compound has unique chemical properties. The synthetic route is as follows.

N-Methylmorpholine (10 drops) was added to a mixture of cyanothioacetamide 1 (4.00 g, 0.04 mol) [5] and indole-3-carbaldehyde (5.80 g, 0.04 mol) in 50 mL of 96% EtOH. The mixture was refluxed for 5 min with stirring. After cooling the resulting red solution, the precipitate formed, which was filtered off after 24 h, washed with diethyl ether, and dried. Yield 5.50 g (61%), yellow powder, mp 169-172C (EtOH) (mp 174-176C [37]). IR spectrum, nu, cm-1: 3320 (N-H), 2215 (C?N). 1H NMR spectrum, delta, ppm: 7.15-7.22 m (3H, H-Ar), 7.88-7.93 m (1H, H-Ar), 8.54 d (1H, H2, J = 2.9 Hz), 8.64 s (1H, CH=), 9.01 br.s (1H, CSNH2), 9.44 br.s (1H, CSNH2), 12.24 br.s (1H, NH). 13C NMR spectrum, deltaC, ppm: 104.1 (C-C?N), 108.2 (C3, indole), 115.0 (CH-Ar), 116.9 (C?N), 120.5 (CH-Ar), 122.9 (CH-Ar), 123.8 (CH-Ar), 129.7 (C-Ar), 135.0 (C-Ar), 138.7 (C-Ar), 142.1 [CH=C(C?N)], 190.3 (C=S). Found, %: C 63.57; H 4.12; N 18.33. C12H9N3S. Calculated, %: C 63.41; H 3.99; N 18.49.

The chemical industry reduces the impact on the environment during synthesis 2-Cyanothioacetamide. I believe this compound will play a more active role in future production and life.

Reference:
Article; Dotsenko; Krivokolysko; Krivokolysko; Frolov; Russian Journal of General Chemistry; vol. 88; 4; (2018); p. 682 – 688; Zh. Obshch. Khim.; vol. 88; 4; (2018); p. 599 – 605,7;,
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Synthetic Route of 261762-98-5, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 261762-98-5, name is 3-Chloro-2-fluorophenylacetonitrile, This compound has unique chemical properties. The synthetic route is as follows.

1-Bromomethyl-3-chloro-2-fluoro-benzene (10.00 g, 44.80 mmol) and KCN (5.80 g, 89.07 mmol) were mixed in DMF and the resulting reaction mixture was stirred at 75 C. for 2 days. The reaction mixture was cooled to room temperature, and water was added. The mixture was extracted with Et2O (3¡Á300 mL). The combined organic phases were washed with H2O (2¡Á200 mL) and brine (1¡Á200 mL), then dried over MgSO4 and concentrated. The crude nitrile was taken up in water and KOH (5.00 g, 89.11 mmol) was added. The resulting mixture was refluxed for 14 hours. After cooling to room temperature, the reaction mixture was diluted with water and washed with Et2O (2¡Á150 mL). The aqueous layer was acidified with concentrated HCl and was extracted with Et2O (3¡Á300 mL). The combined organic phases were washed with H2O (2¡Á200 mL) and brine (1¡Á200 mL), then dried over MgSO4 and concentrated to afford the title acid.

The chemical industry reduces the impact on the environment during synthesis 3-Chloro-2-fluorophenylacetonitrile. I believe this compound will play a more active role in future production and life.

Reference:
Patent; Allerghan, Inc.; US2008/194650; (2008); A1;,
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Related Products of 77-57-6,Some common heterocyclic compound, 77-57-6, name is 1-Phenylcyclopentanecarbonitrile, molecular formula is C12H13N, 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 solution of 1 -phenyl- l-cyclopentanecarbonitrile (1.500 mL, 8.76 mmol, Acros Organics USA) in MeOH (40 mL) was added a solution of palladium, 10wt. % on activated carbon (93 mg, 0.876 mmol, Aldrich) in EtOAc (0.5 mL) and concentrated HCl (0.4 mL). The reaction mixture was stirred at room temperature under H2 (42 psi) overnight. The reaction mixture was filtered through celite, washed the filter-cake with MeOH. The combined filtrates were concentrated and H2O was added to the residue. The aqueous solution was extracted with EtOAc. The aqueous layer was basified (pH >10) using saturated aqueous NaHCtheta3 and extracted with EtOAc. The combined organic extracts were dried over MgSO4, concentrated, and dried in vacuum to give (l-phenylcyclopentyl)methanamine as light yellow oil, which was used in the next step without purification.

The synthetic route of 77-57-6 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; AMGEN INC.; WO2009/137404; (2009); A1;,
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2042-37-7, name is 2-Bromobenzonitrile, belongs to nitriles-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. Product Details of 2042-37-7

Intermediate Example Int3.1(6-Bromo-[1 ,2,4]triazolo[1 ,5-a]pyridin-2-yl)-o-cyanophenyl-amineTo a stirred solution of 213 mg (1 mmol) Int1.2 in THF (2.5 mL) was added 364 mg (2 mmol, 2 eq) 2-Brombenzonitril, 183 mg (0.2 mmol, 0.2 eq) Pd2(dba)3, 374 mg (0.6 mmol, 0.6 eq) rac-BINAP and 240 mg (2.5 mmol, 2.5 eq) NaOtBu at room temperature in a microwave reactor. The solution was heated at 150 C for 50 min under microwave irradiation. After cooling, the solution was filtered and evaporated. Subsequent purification by by preparative reverse phase HPLC gave 186 mg (59 %) of the title compound.1H-NMR (300 MHz, d6-DMSO): delta = 9.56 (1H, s), 9.16 (1 H, s), 7.91 (1 H, d), 7.72 (1 H, d), 7.70 (1 H, d), 7.62 (1H, dd) 7.54 (1 H, d), 7.15 (1H, dd) ppm. UPLC-MS: RT = 1.15 min; m/z (ES+) 315.2 [MH+]; required MW = 314.2.

The synthetic route of 2042-37-7 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; BAYER SCHERING PHARMA AKTIENGESELLSCHAFT; SCHULZE, Volker; KOPPITZ, Marcus; KOSEMUND, Dirk; SCHIROK, Hartmut; BADER, Benjamin; LIENAU, Philip; WENGNER, Antje; BRIEM, Hans; HOLTON, Simon; SIEMEISTER, Gerhard; PRECHTL, Stefan; BOeMER, Ulf; WO2011/63908; (2011); A1;,
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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 67515-59-7 as follows. category: nitriles-buliding-blocks

To a solution of 4-fluoro-3-(trifluoromethyl)benzonitrile (10 g), /-PrOH (8.15 mL) in tetrahydrofuran (THF) (90 mL) stirred under nitrogen at -10 C was added solid NaH (3.46 g) portionwise during 30 min. The reaction mixture was stirred at -10 C for 6 h. The reaction mixture was quenched with water, partitioned between ether (.100 mL) and water (50 mL).The organic phase was dried over magnesium sulphate and evaporated in vacuo to give the crude product 4-[(1-methylethyl)oxy]-3- (trifluoromethyl)benzonitrile (D10) (15 g).

According to the analysis of related databases, 67515-59-7, the application of this compound in the production field has become more and more popular.

Reference:
Patent; GLAXO GROUP LIMITED; DENG, Guanghui; LIN, Xichen; REN, Feng; ZHAO, Baowei; WO2011/134280; (2011); A1;,
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