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New organic compounds containing nitrogen and phosphorus and their manufacture

机译:含氮和磷的新型有机化合物及其制造

摘要

The invention comprises compounds of the general formula: FORM:0792595/IV (b)/1 in which R, R2, R3 and R4 each represent hydrogen or an organic radical, at least one of R2 and R3 being an organic radical, R1 is the residue of an alcohol, R5 is the residue of an alcohol different from that of R1, and -N(R3)(R2) may also represent the ring structure of morpholine or piperidine, and salts and quaternary ammonium salts of the compounds. The compounds may be obtained by reacting an asymmetrical phosphite ester of the formula (R1O)(R5O)P(O).H with (a) an aldehyde or ketone of the formula (R)(R4)CO and an amine of the formula (R3)(R2)NH, or (b) an a -alkylolamine of the formula: FORM:0792595/IV (b)/2 or (c) an alkylidene diamine of the formula: FORM:0792595/IV (b)/3 or (d) an N-disubstituted aminomethyl ether of the formula (R2)(R3)N.CH2.O.CH3 or (e) an aldimine or ketimine of the formula (R)(R4)C = N.R2, methods (c) and (d) being applicable only to the production of compounds in which R4 and R are hydrogen, and method (e) being applicable only to the production of compounds in which R3 is hydrogen. If desired, the resulting product is converted into a salt or, when it contains a tertiary amino group, is quaternated. The residue R1 may be aliphatic or cycloaliphatic, e.g. methyl, ethyl or propyl, and the residue R5 may be aliphatic, cycloaliphatic, araliphatic or heterocyclic, examples of the residue R5 being ethyl, propyl, isopropyl, butyl, hexyl, 2-ethylbutyl, actyl, 2-butyloctyl, dodecyl, octadecenyl, octadecyl, allyl, 2-chlorethyl, benzyl, cyclohexyl and tetrahydrofurfuryl groups. R5 may also be a radical containing thiocyano, cyano or ether groups or halogen atoms. The preferred dialkyl phosphite starting materials are those in which R1 is the residue of a C1-C4 aliphatic alcohol and R5 is the residue of a C8-C30 aliphatic alcohol. Specified aldehydes or ketones of the formula (R)(R4)CO are formaldehyde, acetaldehyde, propionaldehyde, acetone, methyl ethyl ketone, benzaldehyde, substituted benzaldehydes, acetophenone and furfural. Specified amines of the formula (R2)(R3)NH are dimethyl, diethyl, diisopropyl, dibutyl and dicyclohexyl amines, methylamine, ethylamine, butylamine, aniline, p-anisidine, N-ethylaniline, b -phenyl ethylamine, morpholine and piperidine. The compounds used in methods (b) to (e) may be derived from the above mentioned aldehydes or ketones and amines. Reactions (a) and (b) may be carried out without solvents and are preferably effected at 40-100 DEG C. Specified agents which may be used to quaternate the products when they contain a tertiary amino group are methyl iodide, ethyl bromide, isopropyl chloride, secondary butyl bromide, dodecyl bromide, epichlorhydrin, dimethylsulphate, benzyl halides and benzyl halides substituted by halogen atoms or by alkyl or alkoxy groups, e.g. benzyl chloride and p-chlorobenzyl chloride, mennaphthyl chloride, toluene sulphonic acid esters, e.g. the methyl ester, halogen alkyl or halogenaralkylsulphonic acids, e.g. bromethane sulphonic acid and benzyl chloride disulphonic acid. When salts of tertiary amines are used alkylene oxides such as ethylene oxide, propylene oxide or glycide may be used to effect quaternation. The quaternation may be carried out by heating the components at raised temperature, e.g. 50-200 DEG C., if desired, under pressure and an inert solvent may be present. In examples: (1) the compound of the formula (C12H25O)(C2H5O) P.(O)CH2.N(CH3)2 is obtained by reacting formaldehyde with dodecyl ethyl phosphite and an alcoholic solution of dimethylamine at 50-60 DEG C.; (2) the product of (1) is quaternated by treatment with dimethyl sulphate in solution in ether. Benzyl chloride may be used instead of dimethylsulphate to effect the quaternation. The products are stated to be useful as pest control agents, as assistants in the textile, leather or paper industries, e.g. as washing, wetting or foaming agents, and as additives to paints or lubricants. They can also be used as emulsifying or dispersing agents.
机译:本发明包含通式的化合物,其中R,R2,R3和R4各自代表氢或有机基团,R2和R3中的至少一个是有机基团, R1是醇的残基,R5是不同于R1的醇的残基,并且-N(R3)(R2)也可以代表吗啉或哌啶的环结构,以及该化合物的盐和季铵盐。化合物可以通过使式(R1O)(R5O)P(O).H的不对称亚磷酸酯与(a)式(R)(R4)CO的醛或酮和式(I)的胺反应而获得(R3)(R2)NH或(b)式为或(c)式为或(d)式(R2)(R3)N.CH2.O.CH3的N-二取代氨基甲基醚或(e)式(R)(R4)C的醛亚胺或酮亚胺N.R2,方法(c)和(d)仅适用于其中R4和R为氢的化合物的生产,方法(e)仅适用于其中R3为氢的化合物的生产。如果需要,将所得产物转化为盐,或者当其含有叔氨基时,将其季铵化。残基R 1可以是脂族或脂环族的,例如C 1-8。残基R5可以是脂族,脂环族,芳脂族或杂环,残基R5的实例是乙基,丙基,异丙基,丁基,己基,2-乙基丁基,Actyl,2-丁基辛基,十二烷基,十八碳烯基,十八烷基,烯丙基,2-氯乙基,苄基,环己基和四氢糠基。 R 5也可以是含有硫氰基,氰基或醚基或卤素原子的基团。优选的亚磷酸二烷基酯原料是其中R1为C1-C4脂族醇的残基且R5为C8-C30脂族醇的残基的原料。式(R)(R4)CO的特定醛或酮是甲醛,乙醛,丙醛,丙酮,甲基乙基酮,苯甲醛,取代的苯甲醛,苯乙酮和糠醛。式(R2)(R3)NH的特定胺为二甲基,二乙基,二异丙基,二丁基和二环己基胺,甲胺,乙胺,丁胺,苯胺,对苯胺,N-乙基苯胺,b-苯基乙胺,吗啉和哌啶。方法(b)至(e)中使用的化合物可以衍生自上述醛或酮和胺。反应(a)和(b)可以在没有溶剂的情况下进行,并且优选在40-100℃下进行。当含有叔氨基时可以用来季铵化产物的试剂是甲基碘,溴代乙基,异丙基。氯,仲丁基溴化物,十二烷基溴化物,表氯醇,二甲基硫酸盐,苄基卤和被卤素原子或烷基或烷氧基取代的苄基卤苄基氯和对氯苄基氯,甲萘基氯,甲苯磺酸酯,例如甲酯,卤代烷基或卤代芳烷基磺酸,例如溴甲烷磺酸和苄基氯二磺酸。当使用叔胺的盐时,可以使用环氧烷,例如环氧乙烷,环氧丙烷或乙交酯来进行季铵化。季铵化可通过在升高的温度下,例如,在室温下加热组分来进行。如果需要,可在50-200℃的压力下进行,并且可以存在惰性溶剂。在实施例中:(1)式(C12H25O)(C2H5O)P.(O)CH2.N(CH3)2的化合物是通过使甲醛与亚磷酸十二烷基乙酯和二甲胺的醇溶液在50-60℃下反应而获得的。 。; (2)通过在醚溶液中的硫酸二甲酯处理将(1)的产物季铵化。可以使用苄基氯代替硫酸二甲酯来进行季铵化。据称该产品可用作害虫防治剂,在纺织,皮革或造纸工业中用作助剂,例如作为洗涤,润湿或发泡剂,以及作为油漆或润滑剂的添加剂。它们也可以用作乳化剂或分散剂。

著录项

  • 公开/公告号GB792595A

    专利类型

  • 公开/公告日1958-04-02

    原文格式PDF

  • 申请/专利权人 CIBA LIMITED;

    申请/专利号GB19550006508

  • 发明设计人

    申请日1955-03-04

  • 分类号A01N57/18;C07F9/40;C10L1/26;D21H17/10;

  • 国家 GB

  • 入库时间 2022-08-23 20:25:38

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