Iodides-buliding-blocks

These common heterocyclic compound, 619-58-9, name is 4-Iodobenzoic acid, 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. category: iodides-buliding-blocks

General procedure: A typical method for preparation of phenols: A Schlenk test tube with a magnetic stirring bar was charged with CuSO4·5H2O (13 mg, 5 mol %), NaAsc (20 mg, 10 mol %), benzene halide (1.0 mmol), KOH (168-336 mg, 3.0-6.0 equiv) in DMSO/H2O (v/v=1:1, 3.0 mL) at 120 C for 24h. After cooling to room temperature, carefully acidified with dilute aqueous HCl to pH=2-3 and the mixture were stirred for half hour. Then the resultant mixture was extracted with EtOAc (3×20 mL). The combined organic layers were washed with brine (20 mL) and dried over Na2SO4. Purification via silica gel column chromatography with a mixture of ethyl acetate/petroleum ether. Details as follows:

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

Reference:
Article; Song, Guang-Lin; Zhang, Zhang; Da, Yu-Xia; Wang, Xi-Cun; Tetrahedron; vol. 71; 46; (2015); p. 8823 – 8829;,
Iodide – Wikipedia,
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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. 355-43-1, name is 1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-6-iodohexane, A new synthetic method of this compound is introduced below., Formula: C6F13I

In reaction kettleF (CF2) 6-I(1298.5 kg, 2.911 kmol)Was stirred and stirred.Next, Parroyl IPP[Half-life temperature: 40.3 C]AE-3000 so that 20% by massSolution dissolved in (1,1,2,2-tetrafluoroethyl-2,2,2-trifluoroethyl ether)(17.0 kg, 0.017 kmol)And CH2 = CHCH2 (CH2) 5H (336.5 kg, 2.999 kmol)It was dripped at the said reaction kettle.During dripping,The internal temperature was kept at 88-100 C.After completion of drippingKeep the internal temperature at 90-100 C,As a result of analyzing the reaction crude liquid A1 obtained by further stirring for 0.5 hour or more by gas chromatography,It was confirmed that F (CF2) 6CH2CHICH2 (CH2) 5H was contained.From the obtained reaction crude liquid A1,Under reduced pressure (-0.093 kPaG.Less than,Gauge pressure,?G? is added after ?kPa? or ?MPa?. )AE-3000 and excessCH2 = CHCH2 (CH2) 5HIs distilled off,Reaction solution 1a containing F (CF2) 6CH2CHICH2 (CH2) 5H(1622.4 kg) was obtained.

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; AGC glass company; Maeda, Yutaka; Mitsui, Yoshiyuki; Yamane, Shingo; (11 pag.)JP2019/108319; (2019); A;,
Iodide – Wikipedia,
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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. 6940-76-7, name is 1-Chloro-3-iodopropane, This compound has unique chemical properties. The synthetic route is as follows., Application In Synthesis of 1-Chloro-3-iodopropane

EXAMPLE 2; 4-Hydroxy-4-methyl-cyclohexanecarboxylic acid (3-chloro-4-methyl-phenyl)-{3-[5-(4,6-dimethyl-pyrimidine-5-carbonyl)-hexahydro-pyrrolo[3,4-c]pyrrol-2-yl]-propyl}-amide, trifluoroacetate salt (I-16); Step 1-; A mixture of aniline (1 mL, 11.1 mmol), 1-chloro-3-iodo-propane (1.31 mL, 12.2 mmol) and Cs2CO3 (10.8 g, 33.3 mmol) in DMF (15 mL) was stirred at RT overnight. It was diluted with water and extracted with hexane. The organic layer was dried (Na2SO4), filtered and evaporated in vacuo. The residue was purified via SiO2 chromatography eluting with hexane/EtOAc, (95/5) to afford 2.52 g (67%) of 19a (Ar=Ph) as an oil: M+H=170.

According to the analysis of related databases, 6940-76-7, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Roche Palo Alto LLC; US2007/191406; (2007); A1;,
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

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. 626-01-7, name is 3-Iodoaniline, A new synthetic method of this compound is introduced below., Formula: C6H6IN

General procedure: A mixture of substituted aniline (2 mmol), ethyl acetoacetate (1 mmol),RuCl3.3H2O (15 mol%), and ethanol (5 mL) were stirred in a 10 mLround bottom flask at room temperature. After 20 minutes substitutedbenzaldehyde (2 mmol) was added and the reaction mixture was stirredfor the time indicated in Table 3, while being followed by TLC. Aftercompletion of the reaction, the thick precipitate was filtered off andwashed with ethanol (3 × 5 mL) to give the pure product 4.

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:
Article; Mohammadi, Sedigheh; Abbasi, Mohsen; Journal of Chemical Research; vol. 39; 2; (2015); p. 123 – 126;,
Iodide – Wikipedia,
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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. 627-31-6, name is 1,3-Diiodopropane(stabilized with Copper chip), This compound has unique chemical properties. The synthetic route is as follows., Recommanded Product: 627-31-6

To a suspension of potassium 1,3-dioxoisoindolin-2-ide (3 g, 16.2 mmol) in DMF (150 mL) was added 1,3-diiodopropane (4.2 mL, 36.4 mmol) dropwise and heated at 85C for 2 h. The reaction mixture was monitored by LCMS. The reaction mixture was diluted with cold water and extracted with diethyl ether (2×250 mL). The combined organic layer was washed with water (3×200 mL) and brine (250 mL). The organic layer was dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by chromatography with 10% EtOAc in hexane as eluent to afford 3 g of 2-(3-iodopropyl) isoindoline-1,3-dione.

According to the analysis of related databases, 627-31-6, the application of this compound in the production field has become more and more popular.

Reference:
Patent; MEDIVATION TECHNOLOGIES, INC.; MCCULLAGH, Emma; BERNALES, Sebastian; HUNG, David; (415 pag.)WO2017/19822; (2017); A1;,
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

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 1829-28-3 as follows. Recommanded Product: 1829-28-3

In a typical run, 4-isopropylphenylboronic acid (200 mg, 1.22 mmol) was taken up in 4 mL of DMF along with ethyl 2-iodobenzoate, [1,1 ‘-bis(diphenylphosphino)- ferrocene]dichloropalladium (II) complex with CH2Cl2 (149 mg, 15 molpercent) and anhydrous Na2CO3 (194 mg, 1.83 mmol). The reaction mixture was heated in a microwave reactor at 140 0C for 45 min. It was then cooled to room temperature and diluted with EtOAc. The organic layer was washed with water, dried (Na2SO4) and concentrated under reduced pressure to afford crude ethyl 4’-isopropylbiphenyl-2-carboxylate.

According to the analysis of related databases, 1829-28-3, the application of this compound in the production field has become more and more popular.

Reference:
Patent; SIRTRIS PHARMACEUTICALS, INC.; WO2008/100423; (2008); A1;,
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

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. 260355-20-2, name is 1-Chloro-4-iodo-2-(trifluoromethyl)benzene, A new synthetic method of this compound is introduced below., Application In Synthesis of 1-Chloro-4-iodo-2-(trifluoromethyl)benzene

1-Chloro-4-iodo-2-trifluoromethylbenzene (10 mmol) obtained in Reaction 1.2 was dissolved in 20 ml of toluene.Bis(pyridin-2-ylmethyl)amine (12 mmol) was added sequentially to the system.Palladium acetate (0.5 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (12 mmol), 3 ml of triethylamine, stirred for 10 minutes,Add 10 ml of an aqueous solution of cesium carbonate (10 mmol) and heat to 50 C for 4 hours.After the reaction was completed, 20 ml of water was added to the system, and the mixture was stirred for 20 minutes, and the organic phase was dried over anhydrous sodium sulfate, concentrated, and purified by flash column chromatography.3.3 g of yellow 4-chloro-N,N-bis(pyridinyl-2-methyl)-3-trifluoromethylaniline powder was obtained in a yield of 87.5%.

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; Jingfan; Jing Fan; Ge Baoyin; Zhang Ruwei; (7 pag.)CN108633884; (2018); A;,
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Electric Literature of 153898-63-6, These common heterocyclic compound, 153898-63-6, name is 2-Iodo-5-methoxyaniline, 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.

Bis(triphenylphosphine)palladium(ll) dichloride (32,1 mg; 45,8 muiotatauiotaomicronIota), copper(l) iodide (17,8 mg; 91,5 muiotatauiotaomicronIota), 2-lodo-5-methoxyaniline (1,2 g; 4,6 mmol), phenylacetylene (573 ml; 5,5 mmol), and diethylamine (10 ml) are refluxed for 2 h. The residue is chromatographed on silica gel (heptane/EE, 10/1) to afford 5-methoxy-2-(phenylethynyl)aniline (818 mg; 3.7 mmol; 80% of theory). 1H NMR (500 MHz, Chloroform-d) delta 7.54 (d, J = 6.7 Hz, 2H), 7.36 (q, J 8.9, 7.7 Hz, 2H), 7.32 (q, J = 8.9, 8.5 Hz, 2H), 6.34 (dd, J = 8.5, 2.4 Hz, 1H), 6.30 (d, J = 2.3 Hz, 1H), 3.82 (s, 3H).

Statistics shows that 2-Iodo-5-methoxyaniline is playing an increasingly important role. we look forward to future research findings about 153898-63-6.

Reference:
Patent; MERCK PATENT GMBH; DOBELMANN-MARA, Lars; RIEDMUELLER, Stefan; SCHRAUB, Martin; (166 pag.)WO2018/149853; (2018); A1;,
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Related Products of 58313-23-8,Some common heterocyclic compound, 58313-23-8, name is Ethyl-3-iodobenzoate, molecular formula is C9H9IO2, 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.

Ethyl 3-iodobenzoate (939mg, 3.4Ommol) was dissolved in DIVIF (2mL) and a solution of 3-cyanophenylboronic acid (500mg, 3.4Ommol) in DIVIF (5mL) was added. A solutionof Pd(OAc)2 (15mg, 0.O68mmol) and Na2CO3 (858mg, 10.2mmol) in water (2mL) wasadded and the reaction mixture was heated at 110C for 2d. The reaction mixture was concentrated in vacuo and partitioned between DCM (1 5OmL) and water (5OmL). The aqueous fraction was extracted with DCM (5OmL) and the combined organic fractions were dried (MgSO4) and concentrated in vacuo. The residue was purified by columnchromatography to give the title compound (767mg, 90%) as a pale yellow liquid.LCMS: ES 252.1 [IVIHf.

The synthetic route of 58313-23-8 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; PROXIMAGEN LIMITED; MEO, Paul; STEWART, Alison; HOBBS, Christopher; WO2014/20351; (2014); A1;,
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

6293-83-0, name is 2-Iodo-4-nitroaniline, belongs to iodides-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. Computed Properties of C6H5IN2O2

General procedure: A mixture of compound2 (1.0 equiv), 10% Pd/C (0.016 equiv), PPh3 (0.125 equiv), CuI (0.02 equiv), and triethylamine (2 equiv) in ethanol (5 mL) was stirred at 25-30 C for 30 min under nitrogen. To this was added iodoarene (3) (1.0 equiv), and the mixture was initially stirred at room temperature for 1 h and then at 70 C for the time indicated in Table 2. After completion of the reaction, the mixture was cooled to room temperature, diluted with EtOAc (50 mL), and filtered through Celite.The organic layers were collected, combined, washed with water (3 30 mL),dried over anhydrous Na2SO4, filtered, and concentrated under low vacuum.The crude residue was purified by column chromatography on silica gel using methanol/dichloromethane to afford the desired product.

The synthetic route of 6293-83-0 has been constantly updated, and we look forward to future research findings.

Reference:
Article; Babu, P. Vijaya; Gorja, Dhilli Rao; Meda, Chandana Lakshmi T.; Deora, Girdhar Singh; Kolli, Sunder Kumar; Parsa, Kishore V.L.; Mukkanti; Pal, Manojit; Tetrahedron Letters; vol. 55; 20; (2014); p. 3176 – 3180;,
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com