СПОСІБ ОДЕРЖАННЯ ГАЛОГЕНМЕТИЛБЕНЗОЇЛЦІАНІДІВ

    公开(公告)号:UA49813C2

    公开(公告)日:2002-10-15

    申请号:UA97063031

    申请日:1995-11-14

    Applicant: BASF AG

    Abstract: ⁁牰捯獥⁳獩搠獩汣獯摥映牯瀠敲慰楲杮栠污杯湥瑡摥洠瑥票敢穮祯祣湡摩獥栠癡湩⁧桴⁥潦浲汵⁡䤨㨩倠ⵈ佃䌭ⱎ椠桷捩⁨䡐猠慴摮⁳潦⁲⁡桰湥汹爠獥⁴畳獢楴畴整⁤祢挠汨牯浯瑥票牯戠潲潭敭桴汹琠慨⁴慭⁹灯楴湯污祬挠牡祲ㄠ㐭漠桴牥爠獥獴‬牦浯栠污杯湥瑡摥洠瑥票敢穮祯档潬楲敤⁳慨楶杮琠敨映牯畭慬⠠䥉㨩倠ⵈ佃䌭⹬吠敨挠浯潰湵⁤慨楶杮琠敨映牯畭慬⠠䥉
獩爠慥瑣摥眠瑩⁨⁡祣湡摩ⵥ敲敬獡湩⁧潣灭畯摮椠桴⁥牰獥湥散漠⁦⁡敌楷⁳捡摩‬灯楴湯污祬椠湡椠敮瑲漠杲湡捩猠汯敶瑮漠⁲楤畬湥ⱴ愠摮琠敨瀠潲畤瑣漠瑢楡敮⁤祢琠楨⁳牰捯獥⁳獩琠敨獩汯瑡摥‮桔⁥慨潬敧慮整⁤敭桴汹戠湥潺汹挠慹楮敤⁳慨楶杮琠敨映牯畭慬⠠⥉愠敲椠灭牯慴瑮椠瑮牥敭楤瑡⁥牰摯捵獴映牯琠敨猠湹桴獥獩漠⁦汰湡⁴牰瑯捥楴敶愠敧瑮⹳਍਍਍

    METHOD FOR PRODUCING OXIME ETHERS
    113.
    发明专利

    公开(公告)号:CA2405763A1

    公开(公告)日:2001-10-18

    申请号:CA2405763

    申请日:2001-04-04

    Applicant: BASF AG

    Abstract: The invention relates to a method for producing oxime ethers of formula (I), in which the substituents R1 and R2 can be identical or different and can respectively represent cyano, alkyl, haloalkyl, cycloalkyl, phenyl and naphthyl and R3 can represent alkyl, by the alkylation of oximes of the formula (II), under alkaline conditions, using an alkylation agent from the group containing alkyl halides, dialkyl sulfates and dialkyl carbonates. The reaction is carried out in a mixture consisting of between 5 and 25 wt.- % polar aprotic solvents, selected from the group containing nitriles, N- alkylpyrrolidones, cyclic urea derivatives, dimethylformamide and dimethylacetamide, between 55 and 95 wt.- % non-polar solvents, selected fro m the group containing aliphatic hydrocarbons, aromatic hydrocarbons, alkyl esters of alkyl carboxylic acid and ethers and between 0 and 25 wt.- % water , whereby the sum of said proportions amounts to 100 %.

    METHOD OF OBTAINING HAOGENOMETHYLBENZOYL CYANIDES

    公开(公告)号:PL180802B1

    公开(公告)日:2001-04-30

    申请号:PL32034395

    申请日:1995-11-14

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP95/04463 Sec. 371 Date May 6, 1997 Sec. 102(e) Date May 6, 1997 PCT Filed Nov. 14, 1995 PCT Pub. No. WO96/16023 PCT Pub. Date May 30, 1996Halomethylbenzoyl cyanides I PH-CO-CN (I) where Ph is phenyl which is substituted by chloromethyl or bromomethyl and may cary 1-4 other rradicals, are prepared from halomethylbenzoyl chlorides II PH-CO-Cl (II), by reacting II with a cyanide-donating compound in the presence of a Lewis acid, if required in an inert organic solvent or diluent, and then isolating the product. The halomethylbenzoyl cyanides I are important intermediates for synthesizing crop protection agents.

    Process for preparing halogenated methyl benzoyl cyanides

    公开(公告)号:AU4116596A

    公开(公告)日:1996-06-17

    申请号:AU4116596

    申请日:1995-11-14

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP95/04463 Sec. 371 Date May 6, 1997 Sec. 102(e) Date May 6, 1997 PCT Filed Nov. 14, 1995 PCT Pub. No. WO96/16023 PCT Pub. Date May 30, 1996Halomethylbenzoyl cyanides I PH-CO-CN (I) where Ph is phenyl which is substituted by chloromethyl or bromomethyl and may cary 1-4 other rradicals, are prepared from halomethylbenzoyl chlorides II PH-CO-Cl (II), by reacting II with a cyanide-donating compound in the presence of a Lewis acid, if required in an inert organic solvent or diluent, and then isolating the product. The halomethylbenzoyl cyanides I are important intermediates for synthesizing crop protection agents.

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