• 제목/요약/키워드: ‘One-pot’ synthesis

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인 몰립덴산을 촉매로 이용한 효과적이고 간단한 퀸옥살린의 One-Pot합성 (Phosphomolybdic Acid-Catalyzed Highly Efficient and Simple One-Pot Synthesis of Quinoxaline)

  • Chaskar, Atul;Padalkar, Vikas;Phatangare, Kiran;Langi, Bhushan;Naik, Pallavi
    • 대한화학회지
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    • 제53권6호
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    • pp.727-730
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    • 2009
  • 촉매로서 인 몰립덴산을 이용하여 일련의 퀸옥살린의 유도체를 높은 수율로 합성하였다. 이 방법의 장점은 실내 온도에서 간단한 조작, HPA 촉매의 재사용, 반응단계의 친환경적인 면이다.

Oxidative Cyclisation Based One-Pot Synthesis of 3-Substituted[1,2,4]triazolo[4,3-b]pyridazines Using Me4NBr/Oxone

  • Ruso, Jayaraman Sembian;Nagappan, Rajendiran;Kumaran, Rajendran Senthil
    • 대한화학회지
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    • 제57권5호
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    • pp.606-611
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    • 2013
  • A facile one-pot syhthesis of 3-substituted triazolopyridazine and thieno-triazolopyridazine derivatives is described. This protocol involves the preparation of heteroaryl hydrazone from the aldehyde and pyridazinohydrazine derivative followed by subjecting the intermediate directly to oxidative cyclization to assemble the desired 1,2,4-triazloe moiety by employing the mixture of Me4NBr and oxone. This condition is efficient and is able to tolerate wide range of functional groups.

Ring Closure of N-(2-Hydroxyethyl)-N'-phenylthioureas:One-Pot Synthesis of 2-Phenylaminothiazolines

  • 김택현;민정기;이규재
    • Bulletin of the Korean Chemical Society
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    • 제21권9호
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    • pp.919-922
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    • 2000
  • The cyclization reaction of N-(2-hydroxyethyl)-N'-phenylthioureas 2 containingambident nucleophile was ex-amined in the combination of a variety ofbases and p-toluenesulfonyl chloride (TsCl).N-(2-Hydroxyeth-yl) thioureas 2 were readily obtained in high yields from the reaction of the corresponding 1,2-aminoalcohols with phenyl isothiocyanate, avoiding the need for O-protection.The use of a one-pot reaction (NaOH/TsCl) was found to be most effective in producing the requisite 2-phenylaminothiazolines (S-cyclization) 3 in the case ofthioureas 2a-2e derived from N-unsubstituted aminoalcohols,while in the thioureas 2f and 2g prepared from N-substituted aminoalcohols the combination of Et3N and TsCl led to the S-cyclization products.

One-Pot Electrochemical Synthesis of Hierarchical Porous Niobium

  • Joe, Gihwan;Shin, Heon-Cheol
    • Journal of Electrochemical Science and Technology
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    • 제12권2호
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    • pp.257-265
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    • 2021
  • In this study, we report niobium (Nb) with hierarchical porous structure produced by a one-pot, HF-free electrochemical etching process. It is proved experimentally that a well-defined hierarchical porous structure is produced from the combination of a limited repetition of pulse etching and high concentration of aggressive anion (i.e., SO42-), which results in hierarchical pores with high order over 3. A formula is derived for the surface area of porous Nb as a function of the hierarchical order of pores while the experimental surface area is estimated on the basis of the electrochemical gas evolution rate on porous Nb. From the comparison of the theoretical and experimental surface areas, an in-depth understanding was gained about porous structure produced in this work in terms of the actual pore shape and hierarchical pore order.

표면 알킬기를 갖는 실리콘 나노입자의 One-Pot 용액환원 합성 (One-Pot Synthesis of Alkyl-Terminated Silicon Nanoparticles by Solution Reduction)

  • 윤태균;조미경;선양국;이정규
    • Korean Chemical Engineering Research
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    • 제49권5호
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    • pp.577-581
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    • 2011
  • 가시광 영역에서 강한 광루미네선스(photoluminescence, PL) 특성이 있는 실리콘 나노입자는, 생물학적 형광 이미징, RGB(red, green, blue) 디스플레이, 포토닉스, 광전소자 등의 응용소재로 개발될 수 있어 많은 연구가 수행되고 있다. 실리콘 나노입자의 광학적 및 물리화학적 특성을 이용한 실용적인 응용 및 개발을 위해서는 그 특성의 조절이 용이한 제조법 개발이 필수적이다. 본 연구에서는 Na(naphthalide)를 환원제로 사용한 용액환원법을 이용하여 한 단계로 입자표면이 알킬기로 안정화된 평균 <10 nm 크기의 실리콘 나노입자를 합성할 수 있는 방안을 시도하였다. 이를 위하여 실리콘 전구체로 알킬기를 포함하고 있는 (Octyl)$SiCl_3$ 단독 또는 (Octyl)$SiCl_3$$SiCl_4$의 혼합물을 사용하여 Si-Cl 결합의 환원을 통한 입자의 형성과 동시에 반응물에 포함된 Octyl 기에 의한 표면 안정화를 한번에 달성할 수 있었다. 합성한 실리콘 입자의 TEM/EDS, FTIR 분석결과 입자의 크기는 <10 nm이며, 표면이 알킬기로 덮여있어 소수성 용제인 헥산에 쉽게 용해되었으며 입자표면은 소량의 산화된 Si-O-Si 그룹을 포함하고 있었다. UV-vis 및 PL 분석결과 표면 알킬기를 포함하는 실리콘 나노입자의 전형적인 광 특성을 보여 간단한 반응단계를 통하여 표면이 Octyl기로 덮인 실리콘 나노입자를 합성할 수 있음을 보였다. 본 연구에서 시도한 합성법을 응용할 경우, 향 후 실리콘 나노입자의 표면에 다양한 기능기를 one-pot으로 도입할 수 있을 것으로 기대된다.

One Pot Synthesis of Novel Cyanopyridones as an Intermediate of Bioactive Pyrido[2,3-d]Pyrimidines

  • Khatri, Taslimahemad T.;Shah, Viresh H.
    • 대한화학회지
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    • 제58권4호
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    • pp.366-376
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    • 2014
  • Synthesis, structural characterization, and biological activity studies of novel pyrido[2,3-d]pyrimidines (10a-h, 11a-h) are described. Cyclization of cynoacetamides (4, 5) with malonitrile (7) and aldehyde (6a-h) via Hantzsch pyridine synthesis afforded cyanopyridones (8a-h, 9a-h), which on cyclization with formic acid under microwave conditions led to the final product. All the reactions are significantly faster and the isolated yields are remarkably higher in microwave conditions compared to the conventionally heated reactions. The compounds were tested in vitro for their antibacterial activity against Escherichia coli, Pseudomonas aeruginosa, Bacillus subtillus, Staphylococcus aureus, and Micrococcus luteus and antifungal activity against Trichphyton longifusus, Candida albicans, Microsporum canis, Fusarium solani. Compounds 10b, 10e, 11b and 11e exhibited good antibacterial and antifungal activities compared with standards.

Synthesis of 5-Chloro-3-[4-(3-diethylaminopropoxy)benzoyl]-2(4-methoxyphenyl)benzofuran as a $\beta-Amyloid$ Aggregation

  • Choi, Hong-Dae;Seo, Pil-Ja;Son, Byeong-Wha;Kang, Byoung-Won
    • Archives of Pharmacal Research
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    • 제26권12호
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    • pp.985-989
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    • 2003
  • An efficient synthesis of 5-chloro-3-[4-(3-diethylaminopropoxy)benzoyl]-2-(4-methoxyphenyl)benzofuran (8), a potent $\beta$-amyloid aggregation inhibitor, is described. 5-Chloro-2-(4-methoxyphenyl)benzofuran (3) was obtained by the one-pot synthesis of 4-chlorophenol with $\omega$(methylsulfinyl)-p-methoxyacetophenone (1) under Pummerer reaction conditions, and it was followed by the desulfurization of the resultant 5-chloro-3-methylthio-2-(4-methoxyphenyl)benzofuran (2e). Acylation of benzofuran 3 with 4-(3-bromopropoxy)benzoyl chloride (6) gave the ketone 7, which was converted into compound 8 by the treatment of diethylamine.

Supramolecular aminocatalysis via inclusion complex: Amino-doped β-cyclodextrin as an efficient supramolecular catalyst for the synthesis of chromeno pyrimido[1,2-b]indazol in water

  • Shinde, Vijay Vilas;Jeong, Daham;Jung, Seunho
    • Journal of Industrial and Engineering Chemistry
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    • 제68권
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    • pp.6-13
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    • 2018
  • Well-modified amino-appended ${\beta}$-cyclodextrin ($AA-{\beta}-CD$) with an amino group at the primary face of the ${\beta}-CD$ was synthesized and used in the catalytic synthesis of chromeno pyrimido[1,2-b]indazol as supramolecular catalysts in water for the first time. $AA-{\beta}-CD$ was characterized by FT-IR, NMR, MALDI-TOF mass spectrometry, and SEM analysis. A possible reaction mechanism featuring molecular complexation was suggested based on 2D NMR (ROESY) spectroscopy, FE-SEM, DSC, and FT-IR. Advantages such as operational simplicity, recyclability of the catalysts, and accessibility in aqueous medium render this protocol eco-friendly.