Reaction product of hydrazine derivatives and carbon dioxide

Patent metadata

Field	Value
Publication number	US-9469603-B2
Application number	US-201414484449-A
Country	US
Kind code	B2
Filing date	Sep 12, 2014
Priority date	Mar 12, 2012
Publication date	Oct 18, 2016
Grant date	Oct 18, 2016

Abstract

The present invention relates to the synthesis of a novel compound, in which liquid hydrazine and the derivatives thereof react with excess carbon dioxide to enable the carbon dioxide to chemically bond to the hydrazine and the derivatives thereof. To this end, high-pressure carbon dioxide is used to synthesize hydrazine and the derivatives thereof to which the carbon dioxide is bonded in a pure form with no water and no by-product. Furthermore, the present invention provides a method for utilizing the above-described compounds by reacting the compounds with carbonyl compounds.

First claim

We claim:

1. An anhydrous hydrazinium carboxylate derivative represented by the following Structural Formula II, which is synthesized by reacting a compound represented by the following Structural Formula I and high-pressure carbon dioxide of 7.4 MPa or higher, and is a stable solid or gel state at a room temperature:

in Structural Formulas I and II, each of R1 and R2 is independently hydrogen; or, one of an aliphatic hydrocarbon group of 1 to 30 carbons, a substituted aliphatic hydrocarbon group of 1 to 30 carbons, a substituted aliphatic carbocyclic group of 1 to 30 carbons, a substituted aliphatic heterocyclic group of 1 to 30 carbons, a substituted aromatic cyclic group of 1 to 30 carbons, or a substituted aromatic heterocyclic group of 1 to 30 carbons; or, one of an aliphatic hydrocarbon group including at least one of Si, O, S, Se, N, P and As, an aliphatic carbocyclic group including at least one of Si, O, S, Se, N, P and As, an aliphatic heterocyclic group including at least one of Si, O, S, Se, N, P and As, or a aromatic heterocyclic group including at least one of Si, O, S, Se, N, P and As.

2. The anhydrous hydrazinium carboxylate derivative of claim 1 , wherein synthesizing the compound of Structural Formula II by reacting the compound represented by Structural Formula I and carbon dioxide is conducted under a solvent-free condition.

3. The anhydrous hydrazinium carboxylate derivative of claim 1 , wherein synthesizing the compound of Structural Formula II by reacting the compound represented by Structural Formula I and carbon dioxide includes Structural Formula II prepared by using one of water, an alcohol of C1 to C12, an ether of C1 to C12, or an aliphatic hydrocarbon of 1 to 30 carbons, a substituted aliphatic hydrocarbon of 1 to 30 carbons, a substituted aliphatic carbocycle of 1 to 30 carbons, a substituted aliphatic heterocyclic of 1 to 30 carbons, a substituted aromatic cycle of 1 to 30 carbons, and a substituted aromatic heterocycle of 1 to 30 carbons; or a mixed solvent thereof.

4. The anhydrous hydrazinium carboxylate derivative of claim 1 , wherein the compound represented by Structural Formula I includes water.

5. The anhydrous hydrazinium carboxylate derivative of claim 4 , wherein a content of the water included in the compound represented by Structural Formula I is from 1 wt % to 95 wt % with respect to a total weight of the compound and water.

6. The anhydrous hydrazinium carboxylate derivative of claim 1 , wherein the compound represented by Structural Formula I does not include water.

7. The anhydrous hydrazinium carboxylate derivative of claim 1 , wherein the carbon dioxide is in a gas or solid (dry ice) state.

8. An anhydrous hydrazinium carboxylate derivative represented by the following Structural Formula III, which is synthesized by reacting a compound represented by the following Structural Formula I and high-pressure carbon dioxide of 7.4 MPa or higher, and is a stable solid or gel state at a room temperature:

in Structural Formulas I and III, each of R 1 and R 2 is independently hydrogen; or, one of an aliphatic hydrocarbon group of 1 to 30 carbons, a substituted aliphatic hydrocarbon group of 1 to 30 carbons, a substituted aliphatic carbocyclic group of 1 to 30 carbons, a substituted aliphatic heterocyclic group of 1 to 30 carbons, a substituted aromatic cyclic group of 1 to 30 carbons, or a substituted aromatic heterocyclic group of 1 to 30 carbons; or, one of an aliphatic hydrocarbon group including at least one of Si, O, S, Se, N, P and As, an aliphatic carbocyclic group including at least one of Si, O, S, Se, N, P and As, an aliphatic heterocyclic group including at least one of Si, O, S, Se, N, P and As, or a aromatic heterocyclic group including at least one of Si, O, S, Se, N, P and As.

9. The anhydrous hydrazinium carboxylate derivative of claim 8 , wherein synthesizing the compound of Structural Formula III by reacting the compound represented by Structural Formula I and carbon dioxide is conducted under a solvent-free condition.

10. The anhydrous hydrazinium carboxylate derivative of claim 8 , wherein synthesizing the compound of Structural Formula III by reacting the compound represented by Structural Formula I and carbon dioxide includes Structural Formula II prepared by using one of water, an alcohol of C1 to C12, an ether of C1 to C12, or an aliphatic hydrocarbon of 1 to 30 carbons, a substituted aliphatic hydrocarbon of 1 to 30 carbons, a substituted aliphatic carbocycle of 1 to 30 carbons, a substituted aliphatic heterocycle of 1 to 30 carbons, a substituted aromatic cycle of 1 to 30 carbons, and a substituted aromatic heterocycle of 1 to 30 carbons; or a mixed solvent thereof.

11. The anhydrous hydrazinium carboxylate derivative of claim 8 , wherein the compound represented by Structural Formula I includes water.

12. The anhydrous hydrazinium carboxylate derivative of claim 11 , wherein a content of the water included in the compound represented by Structural Formula I is from 1 wt % to 95 wt % with respect to a total weight of the compound and water.

13. The anhydrous hydrazinium carboxylate derivative of claim 8 , wherein the compound represented by Structural Formula I does not include water.

14. The anhydrous hydrazinium carboxylate derivative of claim 8 , wherein the carbon dioxide is in a gas or solid (dry ice) state.

15. An anhydrous hydrazinium carboxylate detivative represented by the following Structural Formula IV, which is synthesized by reacting a compound represented by the following Structural Formula I and high-pressure carbon dioxide of 7.4 MPa or higher, and is a stable solid or gel state at a room temperature:

in Structural Formulas I and IV, each of R1 and R2 is independently hydrogen; or, one of an aliphatic hydrocarbon group of 1 to 30 carbons, a substituted aliphatic hydrocarbon group of 1 to 30 carbons, a substituted aliphatic carbocyclic group of 1 to 30 carbons, a substituted aliphatic heterocyclic group of 1 to 30 carbons, a substituted aromatic cyclic group of 1 to 30 carbons, or a substituted aromatic heterocyclic group of 1 to 30 carbons; or, one of an aliphatic hydrocarbon group including at least one of Si, O, S, Se, N, P and As, an aliphatic carbocyclic group including at least one of Si, O, S, Se, N, P and As, an aliphatic heterocyclic group including at least one of Si, O, S, Se, N, P and As, or a aromatic heterocyclic group including at least one of Si, O, S, Se, N, P and As.

16. The anhydrous hydrazinium carboxylate derivative of claim 15 , wherein synthesizing the compound of Structural Formula IV by reacting the compound represented by Structural Formula I and carbon dioxide is conducted under a solvent-free condition.

17. The anhydrous hydrazinium carboxylate derivative of claim 15 , wherein synthesizing the compound of Structural Formula IV by reacting the compound represented by Structural Formula I and carbon dioxide includes Structural Formula II prepared by using one of water, an alcohol of C1 to C12, an ether of C1 to C12, or an aliphatic hydrocarbon of 1 to 30 carbons, a substituted aliphatic hydrocarbon of 1 to 30 carbons, a substituted aliphatic carbocycle of 1 to 30 carbons, a substituted aliphatic heterocycle of 1 to 30 carbons, a substituted aromatic cycle of 1 to

Assignees

• Univ Sogang Res Foundation

Inventors

• Hur Nam Hwi
• Lee Byeong No

Classifications

• C07C271/02 Primary

  Carbamic acids; Salts of carbamic acids (unsubstituted carbamic acid or salts thereof C01B21/12) · CPC title

• C07C251/80

  the carbon skeleton containing rings · CPC title

• C01B32/50

  Carbon dioxide · CPC title

• C07C229/00

  Compounds containing amino and carboxyl groups bound to the same carbon skeleton · CPC title

• C07C281/02

  Compounds containing any of the groups [IMAGE cpc-sch-C07C-0972.gif], e.g. carbazates · CPC title