Day: September 1, 2020

Name is 1,5-Diphenylpenta-1,4-dien-3-one, as a common heterocyclic compound, it belongs to chiral-oxygen-ligands compound, and cas is 538-58-9, its synthesis route is as follows.,538-58-9

General procedure: In a general procedure, dibenzylidene acetone (1 mmol), N,N-dimethylbarbituric acid/barbituric acid/thiobarbituric acid(1 mmol) and 4 mL of ethanol:water (1:1) were taken in a 50 mL round-bottomed flask. 10 mol% of tetrabutyl ammonium bromide (TBAB) was added to the mixture, and the contents were stirred. The reaction mixture was refluxed and the progress of the reaction was monitored by TLC using ethyl acetate:petroleum ether (30:70) as eluent for disappearance of active methylene compounds. After completion of the reaction, the reaction mixture was allowed to cool to room temperature and diluted with water (5 mL). The solid obtained was filtered at pump and washed with water:ethanol (2:1). The product was recrystallized with ethanol. The products were characterized by their spectral data.

With the complex challenges of chemical substances, we look forward to future research findings about 1,5-Diphenylpenta-1,4-dien-3-one

Reference£º
Article; Aggarwal, Komal; Khurana, Jitender M.; Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy; vol. 143; (2015); p. 288 – 297;,
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Name is 1,5-Diphenylpenta-1,4-dien-3-one, as a common heterocyclic compound, it belongs to chiral-oxygen-ligands compound, and cas is 538-58-9, its synthesis route is as follows.,538-58-9

General procedure: A Schlenk tube with a magnetic stir bar charged with alpha,beta-unsaturated carbonyl compounds (0.5 mmol, 1 equiv), tosyl hydrazide (0.6 mmol, 1.2 equiv), NaOH (1.5 equiv), (n-Bu)4NBr (1.5 equiv). The reaction vessel was placed in an 80 C oil bath, and then stirring at this temperature for 10 h. The reaction mixture was then allowed to cool to ambient temperature, and diluted with 20 mL of ethyl acetate, and washed with brine (15 mL), water (15 mL), and then the organic layer was dried over Na2SO4. After concentrated in vacuo, the crude product was purified by column chromatography. The identity and purity of the known product was confirmed by 1H NMR, 13C NMR, and GC-MS.

With the complex challenges of chemical substances, we look forward to future research findings about 1,5-Diphenylpenta-1,4-dien-3-one

Reference£º
Article; Wen, Jun; Fu, Yun; Zhang, Ruo-Yi; Zhang, Ji; Chen, Shan-Yong; Yu, Xiao-Qi; Tetrahedron; vol. 67; 49; (2011); p. 9618 – 9621;,
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Name is 1,5-Diphenylpenta-1,4-dien-3-one, as a common heterocyclic compound, it belongs to chiral-oxygen-ligands compound, and cas is 538-58-9, its synthesis route is as follows.,538-58-9

General procedure: 9-Amino(9-deoxy)-epi-quinine (6.5 mg, 0.02 mmol), divinyl ketone 1 (0.1 mmol), nitromethane (262 muL, 3.0 mmol), Proton-sponge (4.3 mg, 0.02 mmol) and benzoic acid (4.9 mg, 0.04 mmol) were dissolved in chlorobenzene (238muL). After stirred at 40 oC for 144 h, the reaction mixture was purified by flash chromatography on silica gel (EtOAc/petroleum ether).

With the complex challenges of chemical substances, we look forward to future research findings about 1,5-Diphenylpenta-1,4-dien-3-one

Reference£º
Article; Yao, Yongqi; Liu, Yingying; Ye, Ling; Chen, Feng; Li, Xinying; Zhao, Zhigang; Li, Xuefeng; Tetrahedron; vol. 73; 16; (2017); p. 2311 – 2315;,
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

538-58-9, 1,5-Diphenylpenta-1,4-dien-3-one is a chiral-oxygen-ligands compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated,538-58-9

General procedure: To a solution of dialkyl phosphite (0.01 mol) in anhydrous tetrahydrofuran (30 mL),maintained under a nitrogen atmosphere, sodium (0.02 g) was added and the mixture was stirred at roomtemperature until complete dissolution of sodium. Diarylideneketone 1 (0.01 mol) was then added and themixture heated under reflux for 4 h. After cooling, the reaction mixture was diluted with water (50 mL)and extracted with CHCl3 (2 ¡Á 25 mL). The organic phase was dried over Na2SO4 and concentrated undervacuum. The obtained residue was chromatographed on a silica gel column using a mixture of Et2O andhexane 9:1 as an eluent.

As the paragraph descriping shows that 538-58-9 is playing an increasingly important role.

Reference£º
Article; Lamouchi, Imen; Touil, Soufiane; Heterocycles; vol. 94; 5; (2017); p. 894 – 911;,
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Name is (S)-Propane-1,2-diol, as a common heterocyclic compound, it belongs to chiral-oxygen-ligands compound, and cas is 4254-15-3, its synthesis route is as follows.,4254-15-3

General procedure: A 45percent solution of hydrogen bromide in acetic acid (33.0 g, 23.2 mL) was added dropwise over 10 min to 60.3 mmol optically active diol 4a-f with stirring and ice-cooling. The solution was stirred at 0 ¡ãC for 5 min, and next at room temperature for 45 min. Next, water (100 mL) was added, and the mixture was alkalized to pH 8 with solid Na2CO3. The solution was immediately extracted with ethyl ether (5 .x. 60 mL), and the combined extracts were dried over anhydrous Na2SO4. The ether was evaporated, and the product was distilled under reduced pressure or purified by silica gel column chromatography with gradient AcOEt-hexane 9:1.

With the complex challenges of chemical substances, we look forward to future research findings about (S)-Propane-1,2-diol

Reference£º
Article; Poterala, Marcin; Plenkiewicz, Jan; Tetrahedron Asymmetry; vol. 22; 3; (2011); p. 294 – 299;,
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Name is 1,5-Diphenylpenta-1,4-dien-3-one, as a common heterocyclic compound, it belongs to chiral-oxygen-ligands compound, and cas is 538-58-9, its synthesis route is as follows.,538-58-9

General procedure: To a solution of DVK 1 (0.2 mmol) and active methylene 2 (0.24 mmol) was addedt-Bu-P2 (10uL, 10 mol%) via a micro syringe at room temperature. The reactionmixture was stirred for 2-24 h as indicated in Table 2. The solvent was then removedin vacuo and the crude product was purified by flash chromatography on silica gel(PE/EA = 15:1-10:1) to give the desired product 3.

With the complex challenges of chemical substances, we look forward to future research findings about 1,5-Diphenylpenta-1,4-dien-3-one

Reference£º
Article; Li, Yang-Guo; Zhang, Yang; Du, Guang-Fen; Gu, Cheng-Zhi; He, Lin; Letters in Organic Chemistry; vol. 16; 1; (2019); p. 76 – 80;,
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Name is 1,5-Diphenylpenta-1,4-dien-3-one, as a common heterocyclic compound, it belongs to chiral-oxygen-ligands compound, and cas is 538-58-9, its synthesis route is as follows.,538-58-9

General procedure: General procedure: A mixture of 8a (70.3 mg, 0.3 mmol) and 1a (172.2 mg, 0.36 mmol) in DMSO (2.0 mL) was stirred under nitrogen atmosphere for 5 min at room temperature. Then DBU (0.065 mL, 0.45 mmol), followed by DMSO (1 mL), was added and the resulting mixture was heated to 80 C in N2 atmosphere. After the reaction was complete, the mixture was filtered through a thin layer (30 mm) of silica gel (100-200 mesh) and washed with DCM. The filtrate was concentrated under reduced pressure and the residue was purified by flash chromatography (PE/EtOAc=60/1) to afford 11a (72.1 mg, 76%).

With the complex challenges of chemical substances, we look forward to future research findings about 1,5-Diphenylpenta-1,4-dien-3-one

Reference£º
Article; Shu, Zhen-Cao; Zhu, Jian-Bo; Liao, Saihu; Sun, Xiu-Li; Tang, Yong; Tetrahedron; vol. 69; 1; (2013); p. 284 – 292;,
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

Name is (S)-Butane-1,3-diol, as a common heterocyclic compound, it belongs to chiral-oxygen-ligands compound, and cas is 24621-61-2, its synthesis route is as follows.,24621-61-2

The flask was charged with (S) -butane-1,3-diol (1.00 g, 11.10 mmol) in dichloromethane (DCM) (27 mL),Triethylamine (1.347 g, 13.32 mmol),4-Dimethylaminopyridine (0.136 g, 1.110 mmol) and 4-methylbenzene-1-sulfonyl chloride (2.327 g, 12.21 mmol) were added. The reaction was stirred at room temperature for 1 hour.Quench the reaction with saturated NH 4 Cl,Extracted with DCM. The organic portion was dried over MgSO 4, filtered and concentrated under reduced pressure to give a residue which was purified by silica gel chromatography eluting with 0-50% ethyl acetate / heptane to give the product (0. 288 g, 1.179 mmol, yield 10.62%).

With the complex challenges of chemical substances, we look forward to future research findings about (S)-Butane-1,3-diol

Reference£º
Patent; Abbvie Incorporated; Argiriadi, Maria A.; Breinlinger, Eric C.; Chien, Ellen Yulin Tsai; Cowart, Marlon D.; Frank, Kristine E.; Friedman, Michael M.; Hardy, David J.; Herold, J. Martin; Liu, Huaqing; Chu, Wei; Scanio, Marc J.; Schrimpf, Michael R.; Vargo, Thomas R.; Van Epps, Stacy A.; Webster, Matthew P.; Little, Andrew J.; Dunstan, Teresa A.; Katcher, Matthew H.; Schedler, David A.; (232 pag.)JP6557436; (2019); B1;,
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

1,5-Diphenylpenta-1,4-dien-3-one, cas is 538-58-9, it is a common heterocyclic compound, the chiral-oxygen-ligands compound, its synthesis route is as follows.,538-58-9

General procedure: A solution of N,N-dimethyl barbituric acid (1) (2 mmol) and diarylidene acetone derivatives (2a-p) (2 mmol) in 10 mL of dry CH2Cl2 were charged into a 50 mL round bottom flask under inert atmosphere. Et2NH (2.5 mmol) was then added to the reaction mixture and stirred at room temperature for up to 1.5-2 h, until TLC showed complete consumption of both the reactants. After completion of the reaction, the crude product was directly subjected to column chromatography, using 100-200 mesh silica gel and ethyl acetate/n-hexane (2:8, v/v) as an eluent to afford the pure products 3a-p. The solid products were further crystallized from a mixture of CHCl3/n-heptane. 4.2.1 2,4-Dimethyl-7,11-diphenyl-2,4-diazaspiro[5.5]undecane-1,3,5,9-tetraone (3a) Diarylidene acetone 2a (468.2 mg, 2 mmol) reacted with compound 1 (312.1 mg, 2 mmol) according to GP1 yielded white solid spiro-product 3a (765 mg, 1.96 mmol, 98%); mp 125-127 C; 1H NMR (400 MHz, CDCl3) delta: 2.59 and 2.63 (dd, 2H, J = 15.36 Hz, 4.40 Hz, CH2(e)), 2.85 (s, 3H, -NCH3), 3.01 (s, 3H, -NCH3), 3.72 (t, 2H, J = 14.7 Hz, CH2(a)), 3.99 and 4.03 (dd, 2H, J = 14.7 Hz, 4.40 Hz, CH), 7.06-7.08 (m, 4H, Ar-H), 7.21-7.26 (m, 6H, Ar-H); 13C NMR (100 MHz, CDCl3) delta: 27.98, 28.39, 42.99, 50.55, 60.95, 127.56, 128.69, 128.94, 137.17, 149.70, 169.04, 170.71, 208.29; IR (KBr, cm-1) numax = 2959, 2925, 1716, 1675, 1484, 1422, 1381, 1125, 755, 706; [Anal. Calcd for C23H22N2O4: C, 70.75; H, 5.68; N, 7.17; Found: C, 70.69; H, 5.65; N, 7.01]; LC/MS (ESI, m/z): [M+], calculated 390.21, C23H22N2O4 found 390.16; CCDC-1007513.

538-58-9 is used more and more widely, we look forward to future research findings about 1,5-Diphenylpenta-1,4-dien-3-one

Reference£º
Article; Barakat, Assem; Islam, Mohammad Shahidul; Al-Majid, Abdullah Mohammed; Ghabbour, Hazem A.; Fun, Hoong-Kun; Javed, Kulsoom; Imad, Rehan; Yousuf, Sammer; Choudhary, M. Iqbal; Wadood, Abdul; Bioorganic and Medicinal Chemistry; vol. 23; 20; (2015); p. 6740 – 6748;,
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate

1,5-Diphenylpenta-1,4-dien-3-one, cas is 538-58-9, it is a common heterocyclic compound, the chiral-oxygen-ligands compound, its synthesis route is as follows.,538-58-9

Step 1. Under a nitrogen atmosphere, add 8 L of absolute ethanol and 0.112 kg of anhydrous sodium acetate to a glass reactor heated in a water bath.When the system temperature was heated to 68 C, 0.92 kg of dibenzylideneacetone obtained in Example 1 was added.After stirring for 30 minutes, add ice to the water bath heater to quickly cool the system down to 60 C.Then, 0.2 kg of palladium dichloride prepared in Example 1 was added and reacted at 60 C for 2 hours.Funnel filtration gave bis (dibenzylideneacetone) palladium (0);

With the rapid development of chemical substances, we look forward to future research findings about 1,5-Diphenylpenta-1,4-dien-3-one

Reference£º
Patent; Xi’an Kaili New Materials Co., Ltd.; Zhang Jielan; Chen Dan; Yan Pandun; Xiao Dawei; Li Yuefeng; Wan Kerou; (6 pag.)CN110256503; (2019); A;,
Synthesis and Crystal Structure of a Chiral?C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis
Chiral lanthanide(III) complexes of sulphur¨Cnitrogen¨Coxygen ligand derived from aminothiourea and sodium?D-camphor-¦Â-sulfonate