50563-55-8

Usage

Uses

Used in Pesticide Metabolite Synthesis:
N-(2-methoxyethyl)-2,6-xylidine is used as an intermediate in the synthesis of Dimethachlor Ethane Sulfonic Acid Sodium Salt (D460283), a pesticide metabolite pollutant that can be found in groundwater, surface water, and wastewater. This application is crucial for the development of methods to detect and mitigate the presence of such pollutants in water sources, ensuring environmental safety and water quality.

InChI:InChI=1/C11H17NO/c1-9-5-4-6-10(2)11(9)12-7-8-13-3/h4-6,12H,7-8H2,1-3H3

Upstream product

• 87-62-7 2,6-dimethylaniline 
• 10312-83-1 methoxyacetaldehyde 
• 53782-79-9 (E)-4-(pent-3-en-2-yl)morpholine 
• 109-85-3 2-methoxyethylamine 
• 107-02-8 acrolein 
• 73621-38-2 N-(2-methoxyethyl)-2,6-dimethylcyclohex-2-en-1-one-imine 
• 187737-37-7 propene 
• 40790-56-5 2,6-dimethyl-2-cyclohexen-1-one 
• 100129-63-3 N-(2-chloroethoxycarbonyl)-2,6-dimethylaniline 
• 124-41-4 sodium methylate 
• 120368-21-0 N-(2,6-dimethylphenyl)-2-oxazolidinone 

Relevant academic research and scientific papers

ANOMALOUS RING OPENING OF N-ARYL-2-OXAZOLIDINONES BY ANHYDROUS ALKOXIDE:A CONVENIENT PREPARATION OF N-(ALKOXYETHYL)-2,6-DISUBSTITUTED ANILINES

N-(2-Alkoxyethyl)anilines may be prepared by acylation of an N-unsubstituted aniline with 2-chloroethyl chloroformate, ring closure to oxazolidinone, ring opening with alkoxide under anhydrous conditions to a carbamic acid salt, and decarboxylation.This unexpected mode of ring opening is especially useful in the preparation of N-(2-alkoxyethyl)-2,6-disubstituted anilines.

Plant growth regulating agent

2-Chloro-2',6'-dimethyl-N-(2-methoxyethyl)-acetanilide is disclosed as plant growth regulating agent with long lasting activity.

Process for the production of (substituted) 2,6-dimethylanilines

Aniline derivatives of the formula STR1 wherein R is hydrogen, C1 -C4 -alkyl or C1 -C4 -alkyl substituted by C1 -C2 -alkoxy are produced by reacting a N-(3-pent-2-enyl)-derivative of morpholine, piperidine or pyrrolidine with acrolein in the presence of an inert, aprotic solvent or in the absence of a solvent and heating the reaction product obtained to 100°-400° C. in the presence of a hydrogen-transfer catalyst and in the presence of an amine of the formula R--NH2, wherein R has the meaning given above.

Process for the preparation of 2,6-dialkyl-N-alkylanilines

A process for the preparation of 2,6-dialkyl-N-alkylanilines is disclosed, which process comprises the reaction of a 2,6-dialkylaniline with an alkanol at 200° to 350° C. in the presence of a copper-containing catalyst which contains 0.05 to 10% by weight of palladium or platinum.