PROCESS FOR THE PREPARATION OF N-SUBSTITUTED PHENYLCARBAMOYL METHYL THIO PHOSPHONATES

Title compds. I(R = halo, C2-6 alkyl, C1-3 halogenoalkyl, NO2, C1-4 thioalkyl, OCH3; R1,R2,R3 = C1-6 alkyl; X = O, S; n = 1, 2, 3), useful as insecticides and nematocides, were prepd. by the reaction of compds, II and phosphorous compds. III(one of A and B is Cl or Br, the other SY; Y = H or metal c...

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Hauptverfasser: SALLBECK G, WALTERSDORFER A, EMMEL L, HORLEIN G, SCHONOWSKY H
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creator SALLBECK G
WALTERSDORFER A
EMMEL L
HORLEIN G
SCHONOWSKY H
description Title compds. I(R = halo, C2-6 alkyl, C1-3 halogenoalkyl, NO2, C1-4 thioalkyl, OCH3; R1,R2,R3 = C1-6 alkyl; X = O, S; n = 1, 2, 3), useful as insecticides and nematocides, were prepd. by the reaction of compds, II and phosphorous compds. III(one of A and B is Cl or Br, the other SY; Y = H or metal cation). Thus, chloro acetylanilide II(A = Cl) and ammonium salt of phosphorous compds. III(B = SNH4) was stirred in glycolmethylether for 3-5 hr at 50 C to give I.
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I(R = halo, C2-6 alkyl, C1-3 halogenoalkyl, NO2, C1-4 thioalkyl, OCH3; R1,R2,R3 = C1-6 alkyl; X = O, S; n = 1, 2, 3), useful as insecticides and nematocides, were prepd. by the reaction of compds, II and phosphorous compds. III(one of A and B is Cl or Br, the other SY; Y = H or metal cation). Thus, chloro acetylanilide II(A = Cl) and ammonium salt of phosphorous compds. III(B = SNH4) was stirred in glycolmethylether for 3-5 hr at 50 C to give I.</abstract><oa>free_for_read</oa></addata></record>
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subjects ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
CHEMISTRY
METALLURGY
ORGANIC CHEMISTRY
title PROCESS FOR THE PREPARATION OF N-SUBSTITUTED PHENYLCARBAMOYL METHYL THIO PHOSPHONATES
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