IP Library Granted Patent US 10,377,771
Granted Patent B2
US 10,377,771 · App. 15/860,058 · Granted Aug 13, 2019

Nitrated hydrocarbons, derivatives, and processes for their manufacture

Inventors: Daniel M. Trauth (Crystal Lake, IL); George D. Green (Cary, IL); Raymond J. Swedo (Mt. Prospect, IL); Richard L. James (Eros, LA); Ian A. Tomlinson (Midland, MI)
Assignee: ANGUS CHEMICAL COMPANY
C07D498/10A01N43/76A01N43/90C07C201/08C07C201/12C07C205/02C07C205/04C07C205/05C07C205/06C07C205/15C07C205/16C07C205/18C07C215/08C07C215/20C07C215/28C07C215/42C07C239/10C07D263/04C07D263/52C07D498/04C08G18/3271C07C2601/08C07C2601/14C07C2601/18C07C2602/10Y02P20/582
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,377,771
App. No.
15/860,058
Granted
Aug 13, 2019
Kind
B2
Abstract

Provided is a process for the formation of nitrated compounds by the nitration of hydrocarbon compounds with dilute nitric acid. Also provided are processes for preparing industrially useful downstream derivatives of the nitrated compounds, as well as novel nitrated compounds and derivatives, and methods of using the derivatives in various applications.

Claims (18)

1. A compound of formula II-1:

wherein

R 9 is unsubstituted linear C 2 -C 17 alkyl;

R 10 is H, unsubstituted linear C 1 -C 8 alkyl, or CH 2 OH,

or R 9 , R 10 , and the carbon to which they are attached form an eight membered cycloalkyl ring;

provided that

when the compound is selected from formula II-1, if R 10 is H or unsubstituted linear C 1 -C 8 alkyl, the total number of carbons in R 9 and R 10 , together with the carbon to which they are attached, is 5 to 18; or if R 10 is CH 2 OH, R 9 is unsubstituted linear-C 12 -C 13 alkyl; and the compound is not 2-nitro-1-hexanol, 2-nitro-1-heptanol, 2-nitro-1-octanol, 2-methyl-2-nitro-1-pentanol, 2-methyl-2-nitro-1-hexanol, 2-methyl-2-nitro-1-heptanol, or 2-nitro-1-dodecanol.

2. The compound of claim 1 selected from the group consisting of 2 nitro-2-propyl-1-pentanol, 2-nitro-1-nonanol, 2 nitro-2-propyl-1-hexanol, 2-nitro-1-decanol, 2 nitro-2-propyl-1-heptanol, 2 nitro-1-undecanol, 2 nitro-1-tridecanol, 2 nitro-1-tetradecanol, 2 nitro-1-pentadecanol, 2 nitro-1-hexadecanol, 2-nitro-1-heptadecanol, 2 nitro-1-octadecanol, and 2-nitro-1-nonadecanol.

3. The compound of claim 1 selected from the group consisting of 2-methyl-2-nitro-1-octanol, 2-methyl-2-nitro-1-nonanol, 2-methyl-2-nitro-1-decanol, 2-methyl-2-nitro-1-undecanol, 2-methyl-2-nitro-1-dodecanol, 2-methyl-2-nitro-1-tridecanol, 2-methyl-2-nitro-1-tetradecanol, 2-methyl-2-nitro-1-pentadecanol, 2-methyl-2-nitro-1-hexadecanol, 2-methyl-2-nitro-1-heptadecanol, and 2-methyl-2-nitro-1-octadecanol.

4. The compound of claim 1 selected from the group consisting of 2-ethyl-2-nitro-1-butanol, 2-ethyl-2-nitro-1-pentanol, 2-ethyl-2-nitro-1-hexanol, 2-ethyl-2-nitro-1-heptanol, 2-ethyl-2-nitro-1-octanol, 2-ethyl-2-nitro-1-nonanol, 2-ethyl-2-nitro-1-decanol, 2-ethyl-2-nitro-1-undecanol, 2-ethyl-2-nitro-1-dodecanol, 2-ethyl-2-nitro-1-tridecanol, 2-ethyl-2-nitro-1-tetradecanol, 2-ethyl-2-nitro-1-pentadecanol, 2-ethyl-2-nitro-1-hexadecanol, and 2-ethyl-2-nitro-1-heptadecanol.

5. The compound of claim 1 selected from the group consisting of 2-propyl-2-nitro-1-octanol, 2-propyl-2-nitro-1-nonanol, 2-propyl-2-nitro-1-decanol, 2-propyl-2-nitro-1-undecanol, 2-propyl-2-nitro-1-dodecanol, 2-propyl-2-nitro-1-tridecanol, 2-propyl-2-nitro-1-tetradecanol, 2-propyl-2-nitro-1-pentadecanol, and 2-propyl-2-nitro-1-hexadecanol.

6. The compound of claim 1 selected from the group consisting of 2-butyl-2-nitro-1-hexanol, 2-butyl-2-nitro-1-heptanol, 2-butyl-2-nitro-1-octanol, 2-butyl-2-nitro-1-nonanol, 2-butyl-2-nitro-1-decanol, 2-butyl-2-nitro-1-undecanol, 2-butyl-2-nitro-1-dodecanol, 2-butyl-2-nitro-1-tridecanol, 2-pentyl-2-nitro-dodecanol, 2-hexyl-2-nitro-1-undecanol, 2-heptyl-2-nitro-1-decanol, 2-butyl-2-nitro-1-tetradecanol, and 2-butyl-2-nitro-1-pentadecanol.

7. The compound of claim 1 selected from the group consisting of 2-pentyl-2-nitro-1-heptanol, 2-pentyl-2-nitro-1-octanol, 2-pentyl-2-nitro-1-nonanol, 2-pentyl-2-nitro-1-decanol, 2-pentyl-2-nitro-1-undecanol, 2-pentyl-2-nitro-1-tridecanol, and 2-pentyl-2-nitro-1-tetradecanol.

8. The compound of claim 1 selected from the group consisting of 2-hexyl-2-nitro-1-octanol, 2-hexyl-2-nitro-1-nonanol, 2-hexyl-2-nitro-1-decanol, 2-hexyl-2-nitro-1-dodecanol, and 2-hexyl-2-nitro-1-tridecanol.

9. The compound of claim 1 selected from the group consisting of 2-heptyl-2-nitro-1-octanol, 2-heptyl-2-nitro-1-nonanol, 2-heptyl-2-nitro-1-undecanol, and 2-heptyl-2-nitro-1-dodecanol.

10. The compound of claim 1 selected from the group consisting of 2-octyl-2-nitro-1-decanol and 2-octyl-2-nitro-1-undecanol.

11. The compound of claim 1 selected from the group consisting of 2-hydroxymethyl-2-nitro-1-tetradecanol and 2-hydroxymethyl-2-nitro-1-pentadecanol.

12. The compound of claim 1 is 1-hydroxymethyl-1-nitrocyclooctane.

Assignments (3)
CHANGE OF NAME Recorded Feb 27, 2024
From: ANGUS CHEMICAL COMPANY
To: ADVANCION CORPORATION
Reel/Frame 066697/0518 →
PATENT SECURITY AGREEMENT (1ST LIEN) Recorded Dec 1, 2020
From: ANGUS CHEMICAL COMPANY
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 054553/0706 →
PATENT SECURITY AGREEMENT (2ND LIEN) Recorded Dec 1, 2020
From: ANGUS CHEMICAL COMPANY
To: JEFFERIES FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 054553/0719 →
Continuity (4)
Division 14920156 · Oct 22, 2015
Division 12934817
Provisional Application 61045380 · Apr 16, 2008
Related Publication 20180127435A1 · May 10, 2018