IP Library Granted Patent US 11,903,385
Granted Patent B1
US 11,903,385 · App. 18/388,732 · Granted Feb 20, 2024

1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol as an eco-friendly insecticidal agent against

Inventors: Mai Mostafa Khalaf Ali (Al-Ahsa, SA); Hany Mohamed Abd El-Lateef Ahmed (Al-Ahsa, SA); Antar Ahmed Abdelhamid Ahmed (Sohag, EG); Amer A. Amer (Sohag, EG); Mohamed A. Gad (Giza, EG)
Assignee: KING FAISAL UNIVERSITY
A01N33/10A01P7/04A01P17/00C07C213/08C07C213/10
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 11,903,385
App. No.
18/388,732
Granted
Feb 20, 2024
Kind
B1
Abstract

Synthesis of a compound 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol and its use as an insecticidal agent.

Claims (20)

1. An insecticidally acceptable composition comprising an insecticidally effective amount of a 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol compound having the formula I:

2. A method of killing insects comprising applying to said insects or to a target site of insect infestation an insecticidally effective amount of the insecticidally active composition of claim 1 .

3. The method of killing insects of claim 2 , wherein the insects belong to a species Spodoptera littoralis.

4. The method of killing insects of claim 3 , wherein the 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol compound has an LC 50 of about 10.76 mg/L against the species Spodoptera littoralis after 72 hours of treatment.

5. The method of killing insects of claim 3 , wherein the 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol compound has an LC 50 of about 10.76 mg/L against 2 nd instars of larvae of the species Spodoptera littoralis after 72 hours of treatment.

6. The method of killing insects of claim 3 , wherein the 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol compound has an LC 50 of about 16.65 mg/L against 4 th instars of larvae of the species Spodoptera littoralis after 72 hours of treatment.

7. The method of killing insects of claim 2 , wherein the 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol compound is applied to castor leaves.

8. The method of killing insects of claim 2 , wherein about 12.5 to about 1000 ppm of the 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol compound is applied to the insects or to the target site.

9. A method of repelling insects comprising applying to a target site of insect infestation an insect repelling effective amount of the insecticidally active composition of claim 1 .

10. The method of repelling insects of claim 9 , wherein the insects belong to a species Spodoptera littoralis.

11. A method of controlling an insect pest comprising applying to a target site of insect infestation an insect controlling effective amount of the insecticidally active composition of claim 1 .

12. The method of controlling the insect pest of claim 11 , wherein the insect pest belongs to a species Spodoptera littoralis.

13. A method of making a 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol compound, the method comprising:

adding triethanolamine (TEA) dropwise to a mixture of 2-((naphthalen-1-yloxy)methyl)oxirane and butan-1-amine in ethanol to obtain a reaction mixture;

irradiating the reaction mixture;

cooling the reaction mixture to room temperature;

purifying a precipitating product by crystallization using dioxane; and

obtaining the 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol compound.

14. The method of making the 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol compound of claim 13 , wherein the irradiating step is conducted in an MW oven for about 5 minutes.

15. The method of making the 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol compound of claim 13 , wherein the 1-(butyl(2-hydroxy-3-(naphthalen-1-yloxy)propyl)amino)-3-(naphthalen-2-yloxy)propan-2-ol compound is obtained in an about 73% yield.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2024
From: ALI, MAI MOSTAFA KHALAF; AHMED, HANY MOHAMED ABD EL-LATEEF; AHMED, ANTAR AHMED ABDELHAMID; AMER, AMER A.; GAD, MOHAMED A.
To: KING FAISAL UNIVERSITY
Reel/Frame 066062/0124 →