PROCESS FOR PREPARING 4-OXYPHENOXY-ALKANE-CARBOXYLIC ACID DERIVATIVES

    公开(公告)号:KR820000120B1

    公开(公告)日:1982-02-18

    申请号:KR770002109

    申请日:1977-09-07

    Applicant: HOECHST AG

    Abstract: Title compds.[I; R = halogen, CF3, NO2, CH, C1-4 alkyl, C1-4 alkoxy, C1-4 alkyl thio; A= O, S, NH, N-C1-4 alkyl; R1 = H, C1-4 alkyl; Z = -C(O)OR2, C(S)NH2, CN, n = 0,1,2; R2 = H, C1-12 alkyl, C5-6 cyclo alkyl, C3-6 alkenyl, halo- C3-6 alkenyl; R4,R5 = H, C1-6 alkyl, hydroxy-C1-6 alkyl, C5-6 cyclo alkyl, substituted phenyl, having herbicidal property, were prepd. by reacting compd(II) with compd.(III). Thus, the mixt. of 2-(4'-hydroxyphenoxy)-propionic ethyl ester 42g; CaCO3 33.1 g and acetonitrile 300 ml was refluxed for 90 min. 2-Chloro benzimidazole 33.9 g was added, refluxed for 30 hr, filtered and acetonitrile was removed to give 60.7 g I.

    (di)-thiophosphonic acid esters,(di)-thiophosphonic and-phosphoric acid ester amides
    3.
    发明授权
    (di)-thiophosphonic acid esters,(di)-thiophosphonic and-phosphoric acid ester amides 失效
    (DI) - 邻氨基苯甲酸酯,(DI) - 邻氨基苯甲酸和磷酸酯酰胺

    公开(公告)号:US3816456A

    公开(公告)日:1974-06-11

    申请号:US29313272

    申请日:1972-09-28

    Applicant: HOECHST AG

    CPC classification number: C07F9/657154

    Abstract: COMPOUNDS OF THE FORMULA

    4-(R1-P(=X)(-R2)-S-),R3,R4-THIOCHROMAN

    WHERE R1 IS ALKYL OR ALKOXY EACH HAVING FROM 1 TO 4 CARBON ATOMS OR PHENYL; R2 IS ALKOXY HAVING FROM 1 TO 6 CARBON ATOMS IF R1 IS ALKYL OR PHENYL, AMINO, ALKYLAMINO OR DIALKYLAMINO EACH HAVING FROM 1 TO 6 CARBON ATOMS, OR ALKENYLAMINO HAVING FROM 1 TO 4 CARBON ATOMS; R3 IS HYDROGEN OR ALKYL HAVING FROM 1 TO 4 CARBON ATOMS; R4 IS HYDROGEN, ALKYL HAVING HAVING FROM 1 TO 4 CARBON ATOMS; OR HALOGEN; X IS OXYGEN OR SULFUR; ARE USEFUL PESTICIDES IN THE AGRICULTURAL AND VETERINARY FIELDS.

    HERBICIDAL COMPOSITION
    5.
    发明授权

    公开(公告)号:KR820000732B1

    公开(公告)日:1982-05-03

    申请号:KR770000215

    申请日:1977-02-02

    Applicant: HOECHST AG

    Abstract: Title compds. [I; R2 = C1-6 alkyl, C1-6 alkoxy; R3 = C1-6 alkyl; X = O, S; n = 1-3 were prepd. by reaction of II(R4 = halogen) and III(R5 = halogen). 0.6 kg I[(hal)n = 2-F; R2 = OMe; R3 = Me; X = S completly controlled Alopecurus myosuroides, Setaria lutescens, Poa annua, Lolium multiflorum, Echinochloa crus-galli, and other weeds.

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