Simple exploration of 367-21-5

The synthetic route of 367-21-5 has been constantly updated, and we look forward to future research findings.

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. 367-21-5, name is 3-Chloro-4-fluoroaniline, A new synthetic method of this compound is introduced below., Recommanded Product: 367-21-5

To a solution of Compound 56 (5g, 34.3mmol) in dichloromethane (60mL) was added pyridine (4.2ml, 51.5mmol)under ice-cooling, dropwised a solution of bromine (1.8ml, 34.3mmol) in dichloromethane (40mL), the solution wasstirred for 1 hour. To the reaction mixture was added sodium thiosulfate aqueous solution, and extracted with ethylacetate. The organic layer was dried with anhydrous sodium sulfate, and concentrated under reduced pressure. Theresidue was purified by silica gel chromatography (ethyl acetate / hexane) to yield Compound 57 (6.4g, yield: 83%) asan orange solid.LC-MS: m/z=223. [M+H]+

The synthetic route of 367-21-5 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; The University of Tokyo; Tohoku University; Shionogi & Co., Ltd.; NAGANO, Tetsuo; OKABE, Takayoshi; KOJIMA, Hirotatsu; KAWAGUCHI, Mitsuyasu; NUREKI, Osamu; ISHITANI, Ryuichiro; NISHIMASU, Hiroshi; AOKI, Junken; FUJIKOSHI, Chiaki; KATOU, Manabu; ODAN, Masahide; TANAKA, Nobuyuki; TATENO, Yusuke; YAMANE, Junji; (144 pag.)EP3112369; (2017); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Some scientific research about 367-21-5

According to the analysis of related databases, 367-21-5, the application of this compound in the production field has become more and more popular.

Reference of 367-21-5, 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 367-21-5 as follows.

(1) 145.6 g (1.00 mol) of 3-chloro-4-fluoroaniline were dissolved in a mixture of 330 ml of 48% strength hydrobromic acid and 330 ml of water and diazotized by adding a solution of 70.4 g (1.02 mol) of sodium nitrite in 220 ml of water dropwise at 5 C. The diazonium salt solution thus obtained was added dropwise to a mixture of 188 g (1.3 mol) of copper(I) bromide and 400 ml of 48% strength hydrobromic acid at 30-40 C. After conclusion of gas evolution, the produce was extracted using three 300 ml portions of hexane. The extracts were washed twice with 5N sodium hydroxide solution and once with water, dried over sodium sulfate and evaporated. The residue yielded 187.2 g (89%) of 4-bromo-2-chlorofluorobenzene of b.p.10 =73-75 C. with a purity >99% (determined by gas chromatography) on subsequent distillation.

According to the analysis of related databases, 367-21-5, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Hoechst Aktiengesellschaft; US4920212; (1990); A;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Introduction of a new synthetic route about 367-21-5

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 3-Chloro-4-fluoroaniline, its application will become more common.

Related Products of 367-21-5,Some common heterocyclic compound, 367-21-5, name is 3-Chloro-4-fluoroaniline, molecular formula is C6H5ClFN, 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 3-chloro-4-fluoroaniline (5.82 g, 0.04 mol) in CH2Cl2(150 mL), N-bromosuccinimide (7.12 g, 0.04 mol) was added in portions at 0C under stirring. Upon completion of the addition, the resultant was stirred for 30 minutes and filtered. The filtrate was concentrated and purified by silica gel column chromatography to give 2-bromo-5-chloro-4-fluoroaniline (6.16 g, 69% yield). 1H-NMR (400 MHz, CDCl3):delta = 7.234 (d, J = 8.4 Hz, 1H), 6.788 (d, J = 6.4 Hz, 1H), 3.982 (br, 2H). MS m/z [ESI]: 225.9 [M+1].

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 3-Chloro-4-fluoroaniline, its application will become more common.

Reference:
Patent; Chia Tai Tianqing Pharmaceutical Group Co.,Ltd; Centaurus BioPharma Co., Ltd.; Lianyungang Runzhong Pharmaceutical Co., Ltd.; XIAO, Dengming; XU, Xinhe; LIU, Xijie; HU, Yuandong; YU, Honghao; LIU, Zhihua; PENG, Yong; SUN, Yinghui; LUO, Hong; KONG, Fansheng; HAN, Yongxin; SUN, Jian; EP2952510; (2015); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics