IP Library Granted Patent US 12,215,089
Granted Patent B1
US 12,215,089 · App. 18/081,409 · Granted Feb 4, 2025

Energetic compound embodiments and methods of making and using the same

Inventors: David Chavez (Los Alamos, NM); Jesse Sabatini (Bel Air, MD); Pablo Guzmán (Bel Air, MD); Leah Wingard (Landenberg, PA); Eric Johnson (Millington, MD)
Assignees: Triad National Security, LLC; The United States of America, as represented by the Secretary of the Army
C07D271/06C06B25/34
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Quick Facts
Patent No.
US 12,215,089
App. No.
18/081,409
Granted
Feb 4, 2025
Kind
B1
Abstract

Disclosed herein are embodiments of an energetic compound and methods of making and using the same. Energetic compound embodiments disclosed herein exhibit physical and chemical properties that facilitate their use in various applications, such as high energy propellant plasticizers, melt-castable explosives, and the like. Efficient and safe method embodiments for making the disclosed energetic compound embodiments are described herein.

Claims (8)

1. A method, comprising: exposing a bis-oxadiazole product to a nitrating agent to provide a bis-oxadiazole dinitrate, wherein the bis-oxadiazole product has a structure of a formula

wherein each Y independently is aliphatic-OH or aliphatic-OPG, wherein PG is a hydroxyl protecting group and the nitrating agent is HNO 3 .

2. The method of claim 1 , further comprising making the bis-oxadiazole product by combining a diaminoglyoxime product with a carbonyl-containing reagent and a solvent to form a reaction mixture and heating the reaction mixture at a temperature above room temperature.

3. The method of claim 2 , wherein the diaminoglyoxime product has a structure

the carbonyl-containing reagent has a structure of a formula

wherein Z is alkoxy or halogen and Y is aliphatic-OH or aliphatic-OPG, wherein PG is a hydroxyl protecting group, and the solvent is a mixture of DMF and toluene, or a dioxane solvent, or acetonitrile.

4. The method of claim 3 , wherein the method further comprises making the diaminoglyoxime product by combining a di-aldehyde precursor compound with a hydroxylamine.

5. The method of claim 4 , wherein the di-aldehyde precursor compound is oxalaldehyde and the hydroxylamine is NH 2 OH, or an aqueous composition thereof.

Assignments (3)
CONFIRMATORY LICENSE Recorded Apr 17, 2023
From: TRIAD NATIONAL SECURITY, LLC
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 063342/0658 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2023
From: SABATINI, JESSE; GUZMAN, PABLO; WINGARD, LEAH; JOHNSON, ERIC
To: THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY OF THE ARMY
Reel/Frame 062365/0082 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2023
From: CHAVEZ, DAVID
To: TRIAD NATIONAL SECURITY, LLC
Reel/Frame 062365/0100 →
Continuity (2)
Division 16875544 · May 15, 2020
Provisional Application 62849676 · May 17, 2019
References Cited (10)
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US 20190062287A1 · Sabatini et al. · 2019 [cited by applicant]
Fischer et al., Chem. Eur. J., 2014, 20, 6401-6411. [cited by examiner]
Johnson et al., “Bis(l ,2,4-oxadiazole)bis(methylene) Dinitrate: A High-Energy Melt Castable Explosive and Energetic Propellant Plasticizing Ingredient,” [cited by applicant]
Sausa et al., “Density Functional Theory and Experimental Studies of the Molecular, Vibrational, and Crystal Structure of Bis-Oxadiazole-BisMethylene Dinitrate (BOON),” [cited by applicant]
STN Registry Entry for CAS RN 141737-47-5, entered Jun. 12, 1992. [cited by applicant]
STN Registry Entry for CAS RN 2104547-94-4, entered STN Jul. 28, 2017. [cited by applicant]