61706-54-5

Upstream product

• 79-04-9 chloroacetyl chloride 
• 35203-02-2 2,6-dimethyl-N-methylene benzamine 

Downstream Products

• 81140-62-7 2-Chloro-N-(2,6-dimethyl-phenyl)-N-thiocyanatomethyl-acetamide 
• 17493-73-1 2',6'-dimethyl-N-(isopropoxymethyl)-2-chloroacetanilide 
• 67129-08-2 Metazachlor 
• 83447-95-4 2',6'-Dimethyl-N-(2-Methoxy-1-Methylethoxymethyl) 2-Chloroacetanilide 
• 109876-70-2 Diethyl 5-(2,6-dimethylphenyl)-6-oxo-hexahydro-1,3,5-thiadiazepin-2-ylidene-malonate 
• 109876-77-9 {[(2-Chloro-acetyl)-(2,6-dimethyl-phenyl)-amino]-methyl}-dithiocarbamic acid isopropyl ester 
• 109876-68-8 2-(2,6-Dimethylphenyl)-5-isopropyl-6-oxo-4,5,6,7-tetrahydro-1,3,5-thiadiazepine 
• 109876-69-9 2-(2,6-Dimethylphenyl)-6-oxo-5-thioxo-hexahydro-1,3,5-thiadiazepine 
• 109876-67-7 5-(2,6-Dimethylphenyl)-2-methoxy-6-oxo-4,5,6,7-tetrahydro-1,3,5-thiadiazepine 
• 81140-63-8 N-(2,6-Dimethylphenyl),N-isothiocyanatomethyl chloroacetamide 
• 53306-42-6 N-(Acetylamino-methyl)-2-chloro-N-(2,6-dimethyl-phenyl)-acetamide 

Relevant academic research and scientific papers

PROCESS FOR PREPARING ACETANILIDES

The present invention relates to a novel process for preparing acetanilides of the formula (I) by reacting a 2-halo-N-halomethylacetanilide of the formula (II) with an azole of the formula (III) H-A (III) wherein the substituents R, R1, R 2, R 3, R 4, A, X and X1 in the formulae (I), (II) and (III) have the meanings as indicated in the description.

The use of N-dichloroacetyl-1,2,3,4-tetrahydroisoquinolin as antidote for the protection of cultivated plants against damage caused by herbicidally active acetanilides; combinations thus obtained and process for their preparation

The known N-dichloroacetyl-1,2,3,4-tetrahydroisoquinoline of the formula , R represents an optionally substituted N-containing heterocyclic radical,, X and Y are identical or different and represent alkyl,, Z represents halogen, and, , n represents 0, 1 or 2,and their herbicidally active acid addition salts and metal salt complexes, - or of the formula , R1 represents alkyl, halogen, haloalkyl, alkylthio, alkylsulphonyl, aminosulphonyl, cyano or nitro,, R2 and R3 are identical or different and represent hydrogen, alkyl, halogen, haloalkyl or optionally substituted phenyl,, R4 represents alkyl or optionally substituted phenyl, and, , m represents integers from 0 to 5,or of the formula , A represents oxygen, sulphur or the group , R7 represents hydrogen or alkyl,, R8 represents hydrogen, alkyl, haloalkyl, alkenyl, alkynyl, cycloalkyl, halogen, optionally substituted aryl and aralkyl or the groups -OR11, -SR11 and NR10R11,, R10 represents hydrogen, alkyl or optionally substituted aryl,, R11 represents hydrogen, alkyl, haloalkyl, alkenyl, alkynyl, cycloalkyl or optionally substituted aralkyl,, R5 represents alkyl,, R6 represents alkyl or halogen,, R9 represents halogen, and, , p represents the numbers 0, 1 or 2.

N-Dichloroacetyl-1.2.3.4-tetrahydroquinaldine, its preparation and its use in preventing herbicidal injury to cultivated plants

1. Claims for the contracting states : BE, CH, DE, FR, GB, IT, NL N-Dichloroacetyl-1,2,3,4-tetrahydro-quinaldine of the formula see diagramm : EP0006540,P18,F2 1. Claims for the contracting state AT Process for the preparation of N-dichloroacetyl-1,2