Synthesis of trifluoroacetyl fluoride
    4.
    发明授权
    Synthesis of trifluoroacetyl fluoride 失效
    三氟乙酰氟的合成

    公开(公告)号:US4374782A

    公开(公告)日:1983-02-22

    申请号:US275009

    申请日:1981-06-18

    IPC分类号: C07C51/58

    CPC分类号: C07C51/58

    摘要: A process for the preparation of trifluoroacetyl fluoride is disclosed, which comprises reacting, in the liquid phase, hexafluorothioacetone dimer in an aprotic solvent with at least a catalytic amount of an alkali metal fluoride in the presence of an oxidizing agent selected from the group consisting of Ag.sub.2 O, oxides of Pb, Sn, Ni, Co and Fe and M.sub.2 S.sub.2 O.sub.8 wherein M is an alkali metal. The preferred aprotic solvent is dimethylformamide; the preferred alkali metal fluoride is KF; and the preferred oxidizing agents are NiO, PbO.sub.2, and M.sub.2 S.sub.2 O.sub.8 wherein M is Na or K.

    摘要翻译: 公开了一种制备三氟乙酰氟的方法,其包括使液相中的六氟硫代丙酮二聚体在非质子传递溶剂中与至少一种催化量的碱金属氟化物在选自以下的氧化剂存在下反应: Ag2O,Pb,Sn,Ni,Co和Fe的氧化物和M2S2O8,其中M是碱金属。 优选的非质子溶剂是二甲基甲酰胺; 优选的碱金属氟化物为KF; 优选的氧化剂是NiO,PbO2和M2S2O8,其中M是Na或K.

    Process of preparing hexafluorothioacetone dimer
    6.
    发明授权
    Process of preparing hexafluorothioacetone dimer 失效
    制备六氟硫代丙酮二聚体的方法

    公开(公告)号:US4326068A

    公开(公告)日:1982-04-20

    申请号:US216035

    申请日:1980-12-15

    IPC分类号: C07D339/00

    CPC分类号: C07D339/00

    摘要: An improved process for the reaction of hexafluoropropene with elemental sulfur and alkali metal fluoride such as KF, in an aprotic solvent selected from the group consisting of acetonitrile dimethylacetamide, dimethylformamide, dimethyl sulfoxide and N-methyl pyrrolidone under substantially one atmosphere pressure and at tempertures of between about 25.degree. and 100.degree. C. is disclosed. The preferred alkali metal fluoride is KF and the preferred aprotic solvent is dimethylformamide.

    摘要翻译: 一种改进的六氟丙烯与碱性金属氟化物如KF反应的方法,在非质子传递溶剂中,选自乙腈二甲基乙酰胺,二甲基甲酰胺,二甲基亚砜和N-甲基吡咯烷酮,基本上一个大气压和 介于约25℃和100℃之间。 优选的碱金属氟化物是KF,优选的非质子溶剂是二甲基甲酰胺。

    Conversion of 1,1,1-trichloroperhaloalkanes into perhaloalkanoyl
chlorides
    7.
    发明授权
    Conversion of 1,1,1-trichloroperhaloalkanes into perhaloalkanoyl chlorides 失效
    将1,1,1-三氯环烷烃转化为全卤烷酰氯

    公开(公告)号:US4411843A

    公开(公告)日:1983-10-25

    申请号:US372576

    申请日:1982-04-29

    IPC分类号: C07C17/278 C07C51/58

    CPC分类号: C07C17/278 C07C51/58

    摘要: A process for the preparation of perhaloalkanoyl chloride is disclosed which comprises reacting 1,1,1-trichloroperfluoroalkane, with a sulfur trioxide-containing compound selected from the group consisting of oleum sulfur trioxide and stabilized sulfur trioxide in the presence of catalytic amounts of a halogen catalyst selected from the group consisting of iodine, bromine, iodine monobromide and iodine monochloride and bromine monochloride wherein the 1,1,1-trichloroperhaloalkane is a straight or branched chain acyclic organic compound having 2 to 8 carbon atoms and having at least one trihalomethyl group wherein at least one halo atom is fluorine and having the remaining carbon atoms substituted by F, Cl, Br or I atoms.

    摘要翻译: 公开了一种制备全卤烷酰氯的方法,其包括在催化量的卤素存在下使1,1,1-三氯全氟烷烃与选自三氧化硫烟和硫酸三氧化硫的三氧化硫的化合物反应 选自碘,溴,一碘化碘和一氯化碘和一氯化氯的催化剂,其中1,1,1-三氯环烷烃是具有2-8个碳原子并具有至少一个三卤代甲基的直链或支链无环有机化合物 其中至少一个卤原子是氟并且其余的碳原子被F,Cl,Br或I原子取代。

    Process for the preparation of perhaloalkanoyl chloride
    8.
    发明授权
    Process for the preparation of perhaloalkanoyl chloride 失效
    制备全卤烷酰氯的方法

    公开(公告)号:US4340548A

    公开(公告)日:1982-07-20

    申请号:US216033

    申请日:1980-12-15

    IPC分类号: C07C51/58

    CPC分类号: C07C51/58

    摘要: A process for the preparation of perhaloalkanoyl chloride is disclosed which comprises reacting 1,1,1-trichloroperfluoroalkane, with a sulfur trioxide-containing compound selected from the group consisting of oleum sulfur trioxide and stabilized sulfur trioxide in the presence of catalytic amounts of a halogen catalyst selected from the group consisting of iodine, bromine, iodine monobromide and iodine monochloride and bromine monochloride. The preferred product is trifluoroacetyl chloride.

    摘要翻译: 公开了一种制备全卤烷酰氯的方法,其包括在催化量的卤素存在下使1,1,1-三氯全氟烷烃与选自三氧化硫烟和硫酸三氧化硫的三氧化硫的化合物反应 催化剂选自碘,溴,一碘化碘和一氯化碘和一氯化氯。 优选的产物是三氟乙酰氯。

    Conversion of hexafluorothioacetone dimer into hexafluoroacetone
    9.
    发明授权
    Conversion of hexafluorothioacetone dimer into hexafluoroacetone 失效
    六氟硫代丙酮二聚体转化成六氟丙酮

    公开(公告)号:US4337362A

    公开(公告)日:1982-06-29

    申请号:US271456

    申请日:1981-06-08

    申请人: Louis G. Anello

    发明人: Louis G. Anello

    CPC分类号: C07C45/567

    摘要: The production of hexafluoroacetone by contacting, in the liquid phase, hexafluorothioacetone dimer with at least a stoichiometric amount of an aprotic solvent selected from the group consisting of dimethylacetamide, dimethylformamide, dimethyl sulfoxide and N-methyl pyrrolidone and at least a catalytic amount of an alkali metal fluoride or a sulfonic acid having general formula RSO.sub.3 H is disclosed. Dimethylformamide and dimethyl sulfoxide are the preferred aprotic solvents; KF is the preferred alkali metal fluoride; and CH.sub.3 SO.sub.3 H and pCH.sub.3 C.sub.6 H.sub.4 SO.sub.3 H are the preferred sulfonic acids. The production of hexafluoroacetone by contacting hexafluoropropene with elemental sulfur and a catalytic amount of an alkali metal fluoride in an aprotic solvent at a temperature of between about 40.degree. and about 70.degree. C. for a time sufficient to produce hexafluorothioacetone dimer combined with increasing the temperature to between about 90.degree. and 150.degree. C. and maintaining said temperature for a time sufficient to produce hexafluoroacetone is also disclosed.

    摘要翻译: 通过使六氟硫代丙酮二聚体与至少一种选自二甲基乙酰胺,二甲基甲酰胺,二甲基亚砜和N-甲基吡咯烷酮的至少一种化学计量的非质子溶剂和至少一种催化量的碱接触来制备六氟丙酮 公开了具有通式RSO 3 H的金属氟化物或磺酸。 二甲基甲酰胺和二甲基亚砜是优选的非质子溶剂; KF是优选的碱金属氟化物; 和CH 3 SO 3 H和pCH 3 C 6 H 4 SO 3 H是优选的磺酸。 六氟丙烯与元素硫和催化量的碱金属氟化物在非质子传递溶剂中在约40℃至70℃之间的温度下接触足以产生六氟硫代丙酮二聚物与提高温度的时间的六氟丙酮的生产 至约90℃至150℃之间并维持所述温度足以产生六氟丙酮的时间。