Method and catalyst for preparing aniline compounds and use thereof
The present invention provides a method for preparing aniline compounds, and also provides a kind of catalyst and use thereof. This method for synthesizing an aniline compound in the invention includes following steps: use molybdenum oxide and activated carbon as catalyst, hydrazine hydrate as reducing agent, then reduce aromatic nitro compounds to aniline compounds. This method is green and high efficiency, and easy to be applied in industry.
1. A method for preparing aniline compounds, comprising reacting aromatic nitro compounds with hydrazine hydrate in the presence of molybdenum oxide and activated carbon at a molar ratio of the molybdenum oxide to the aromatic nitro compounds from 0.005:1 to 0.05:1 to reduce the aromatic nitro compounds into aniline compounds, wherein the weight ratio of the molybdenum oxide to the activated carbon is from 1:2 to 1:8, whereby a reaction mixture comprising the aniline compounds is obtained.
2. The method according to claim 1 , wherein the molybdenum oxide comprises one or more compounds having the formula MoO x , wherein x is a number between 2 and 3, inclusive wherein when x=2 or 3, the molybdenum oxide is MoO 2 or MoO 3 , and respectively, when x is a non-integer between 2 and 3, the molybdenum oxide has an average valence between +4 and +6.
3. The method according to claim 1 , wherein the molybdenum oxide and the activated carbon are premixed before the reaction.
4. The method according to claim 1 , wherein the molar ratio of the hydrazine hydrate to the aromatic nitro compounds is from 2:1 to 8:1.
5. The method according to claim 1 , wherein the temperature of the reaction is 25° C. to reflux.
6. The method according to claim 1 , wherein
the aromatic nitro compounds have the formula I:
and the aniline compounds have the formula II:
wherein R 1 -R 5 are the same or different from each other and each is selected from the group consisting of a hydrogen atom, halogen atom, C1-C6 alkyl, phenyl and its substituents, benzyl and its substituents, SR 6 , OR 7 , COOR 8 , CONR 9 R 10 and CN; wherein R 6 , R 7 , R 8 , R 9 and R 10 each is selected from the group consisting of a hydrogen atom, C1-C6 alkyl, phenyl and its substituents, and benzyl and its substituents.
7. The method according to claim 1 , wherein the reaction is carried out in the presence of a protic solvent.
8. The method according to claim 1 , wherein the hydrazine hydrate is a hydrazine hydrate aqueous solution with a mass concentration of 40-80%.
9. The method according to claim 1 , further comprising filtering the reaction mixture after reaction, recovering a filter residue from the filtered reaction mixture, and adding the recovered filter residue to the reaction as a recycled catalyst.
10. The method according to claim 7 , wherein the protic solvent is selected from the group consisting of water, methanol, ethyl alcohol, isopropanol, and a combination thereof.