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2,4-二氯-5-羟基苯肼的制备 被引量:1

Preparation of 2, 4-dichloro-5-hydroxy-phenylhydrazine
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摘要 文章选择以2,4-二氯苯酚为起始原料,经羟基保护、硝化、水解、还原、重氮化、还原,成功合成了2,4-二氯-5-羟基苯肼,优化实验条件下六步反应总摩尔收率可达46.6%(以2,4-二氯苯酚计)。产品熔点与文献相符,又经元素分析、红外光谱、核磁共振波谱表征了其结构。 In the paper, various synthetic routes to obtain 2,4-dichloro-5-hydroxyphenylhydrazine were briefly discussed. 2,4-dicholorophenol was chosen as starting material, followed by esterification, natration, hydrolyzation, reduction, diazotization, reduction, the products were obtained. The products were characterized by melting point measurement, fourier transform infrared (FT-IR) and hydrogen nuclear magnetic resonance (H^1-NMR). The melting point of the products was identical with the literature, and the stucture was also confirmed by FT-IR and H-NMR. Throush optimizing the experimental parameters, the molar yields of the final products could reach as high as 46.6 %.
出处 《广东化工》 CAS 2009年第2期26-28,100,共4页 Guangdong Chemical Industry
基金 山东省科技攻关项目(2007GG20003001)
关键词 2 4-二氯-5-硝基苯酚 2 4-二氯-5-羟基苯胺 2 4-二氯-5-羟基苯肼 合成 定位硝化 2,4-dichloro-5-nitrophenol 2,4-dichloro-5-hydroxy-aniline synthesize locality narration 2,4-dichloro-5-hydroxy- phenylhydrazine
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  • 1靳通收,刘利宾,姚剑申,张建设,王爱卿.常温下合成磷酸三苯酯的研究[J].有机化学,2005,25(5):595-597. 被引量:11
  • 2Sagar A D, Shinde N A, Bandgar B P. Microwave-ass isted Synthesis of Triaryl Phosphates[J]. Orj Prep Proced lnt, 2000, 32(3): 26-271.
  • 3Krishnakumar V K. Sthesis of Trial Phosphates by Polyethylene Glycols in a Two-Phase system: Phase-Transfer Catalysis[J]. Synthetic Communications, 1984, 14(2): 189-196.
  • 4Shindo N, Suzuki F, Motohashi F. 2,4-Substituted-5-nitrophenols[P]. JP 7410661, 1974-03-12.
  • 5Avenue Montaigne. Oxadiazolone Compounds and Herbicidal Compositions Containing Them[P]. GB 1063799, 1964-12-1 I.
  • 6Chang J H. Herbicidal 3-isoxazolidinones and hydroxamic acids[P]. US 4405357, 1983-09-20.
  • 7Guiducci M A, Levinson MI. Process for 2-[(2-chlorophenyl)methyl]-4, 4-dimethyl-3-isoxazolidinone[P]. US 4742176, 1988-05-03.
  • 8Hans J D. Process for preparing substituted oxadlazolones[P]. US 5756752, 1998-05-26.
  • 9Roger B. 3-(2,4-dichloro-5-propargyloxy-phenyl)oxadiazolone derivatives useful as herbicides[P]. US 3818026, 1974-06-18.

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