41200-96-8Relevant articles and documents
A method for synthesizing intermediate oxadiazon
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Paragraph 0077; 0087; 0105-0110; 0126-0132; 0148-0152, (2019/07/04)
The invention discloses a method for synthesizing intermediate oxadiazon, comprises the following steps: takes amino phenol as an initial raw material; to m-aminophenol acylation reaction is carried out, thereby obtaining a reaction solution A; the reaction solution A to proceed chlorination reaction, to obtain 2, 4 - dichloro - 5 hydroxy acetanilide; to the 2, 4 - dichloro - 5 hydroxy acetanilide etherification reaction, to obtain 2, 4 - dichloro - 5 isopropoxy acetanilide; to the 2, 4 - dichloro - 5 isopropoxy acetyl aniline to deprotected, get 2, 4 - dichloro - 5 isopropoxyaniline. The invention of 2, 4 - dichloro - 5 - isopropoxy aniline synthesis method to avoid the pollution of the environment, but there are few process steps, high yield.
Solvent-free catalytic hydrogenation method for preparation of 2,4-dichloro-5-isopropoxy aniline
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Paragraph 0008; 0009; 0010; 0011; 0012, (2017/02/17)
The invention especially discloses a solvent-free method for hydrogenation preparation of 2,4-dichloro-5-isopropoxy aniline from 2,4-dichloro-5-isopropoxy nitrobenzene, belonging to the field of catalytic hydrogenation production. The method uses 2,4-dichloro-5-isopropoxy nitrobenzene as a raw material and is characterized in that 2,4-dichloro-5-isopropoxy nitrobenzene reacts with hydrogen at a temperature of 80 to 100 DEG C and a pressure of 0.3 to 2.5 MPa in the presence of a catalyst and an auxiliary agent, no solvent is added, and water is separated after completion of the reaction so as to obtain chloroaniline. The catalyst is a noble metal catalyst prepared through independent research and development, and the usage amount of the catalyst is 0.05 to 20% of the mass of 2,4-dichloro-5-isopropoxy nitrobenzene; the auxiliary agent is a mixture of ethanolamine and pyridine, and the usage amount of the auxiliary agent is 0.01 to 10% of the mass of 2,4-dichloro-5-isopropoxy nitrobenzene; and chromatographic purity of obtained 2,4-dichloro-5-isopropoxy aniline is 99.5% or above, a dechlorination amount can be controlled within 0.1%, a conversion rate is 100%, and yield is 95% or above.
Synthesis and Biological Activity of Cyclic Imide Derivatives and Related Compounds
Ando, Iwao,Ohtsuka, Toshikazu,Miki, Nobuo,Takahashi, Toshio,Hayase, Yoshio,Hayashi, Yoshiyuki
, p. 2001 - 2004 (2007/10/02)
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