.alpha.-(Cyanoethyl)-benzoin ethers
    1.
    发明授权
    .alpha.-(Cyanoethyl)-benzoin ethers 失效
    '((CYANOETHYL)-BENZOIN ETHERS

    公开(公告)号:US3937722A

    公开(公告)日:1976-02-10

    申请号:US416041

    申请日:1973-11-15

    摘要: The invention relates to racemates of the formula (I) ##SPC1##in whichR.sub.1 and R.sub.2 are hydrogen, lower alkyl, methoxy, ethoxy or halogen,R.sub.3 is unsubstituted alkyl or lower alkyl substituted with alkoxy carbonyl carbonamido, cyano or hydroxyl or unsubstituted alkenyl or alkenyl substituted with halogen or halogen-, methyl-, ethyl-, methoxy- or ethoxy-substituted phenyl or unsubstituted cycloalkyl or cycloalkyl substituted with lower alkyl or unsubstituted phenylalkyl or phenylalkyl, the phenyl nucleus of which being substituted with methyl, methoxy, halogen or nitro, andR.sub.4 is unsubstituted alkyl or alkenyl or unsubstituted cycloalkyl or cycloalkyl substituted with lower alkyl or unsubstituted phenyl or phenyl substituted with lower alkyl methoxy, ethoxy or halogen or unsubstituted phenylalkyl or phenylalkyl, the phenyl nucleus of which being substituted with methyl, methoxy or halogen andX is oxygen or sulphur,Which are useful as photosensitizers for light induced polymerisations of vinyl monomers as well as for the light induced crosslinking of unsaturated polycondensates and polymers.

    Preparation of novel fungicidally active spiro derivatives of
3-(3,5-dihalogenophenyl)-oxazolidine-2-thion-4-ones
    7.
    发明授权
    Preparation of novel fungicidally active spiro derivatives of 3-(3,5-dihalogenophenyl)-oxazolidine-2-thion-4-ones 失效
    3-(3,5-二卤代苯基) - 恶唑烷-2-硫杂-4-酮的杀真菌活性螺衍生物的制备

    公开(公告)号:US4291046A

    公开(公告)日:1981-09-22

    申请号:US117134

    申请日:1980-01-30

    CPC分类号: C07D263/52 A01N43/76

    摘要: Fungicidally active novel spiro derivatives of 3-(3,5-dihalogenophenyl)-oxazolidine-2-thion-4-ones of the formula ##STR1## in which X and Y each independently is halogen, andn is 2 or 3,are produced by reacting an .alpha.-hydroxy-cycloalkylcarboxylic acid or acid ester of the formula ##STR2## in which R is hydrogen or alkyl with 1 to 4 carbon atoms,(a) with an isothiocyanate of the formula ##STR3## or (b) with an aniline of the formula ##STR4## in the presence of a diluent, and then cyclizing the .alpha.-hydroxycycloalkyl-carboxylic acid amide formed of the formula ##STR5##

    摘要翻译: 产生其中X和Y各自独立地为卤素且n为2或3的式“IMAGE”的3-(3,5-二卤代苯基) - 恶唑烷-2-硫酮-4-酮的杀真菌活性新型螺衍生物 其中R是氢或具有1至4个碳原子的烷基的α-羟基 - 环烷基羧酸或酸式酯,(a)与下式的异硫氰酸酯或(b)与 苯胺,在稀释剂存在下,然后使由式“IMAGE”形成的α-羟基环烷基 - 羧酸酰胺环化,

    .DELTA.4-Oxazolin-2-ones and process therefor
    8.
    发明授权
    .DELTA.4-Oxazolin-2-ones and process therefor 失效
    {66 4-恶唑啉-2-酮及其制备方法

    公开(公告)号:US4130563A

    公开(公告)日:1978-12-19

    申请号:US770259

    申请日:1977-02-18

    摘要: Compounds having the formula ##STR1## wherein R is hydrogen or an acyl radical are prepared by chlorinating 3-acyl-oxazolidin-2-ones, followed by dehydrochlorination and optionally by saponification and reacylation. The compounds are useful as starting material for substitution and addition reactions and as vinyl monomers in homo- and copolymerizations, whereby oxazolidin-2-one rings containing polymers are formed. These polymers can be used as antistatic agents, dyeing auxiliaries and ion exchangers.

    摘要翻译: 通过氯化3-酰基 - 恶唑烷-2-酮,然后脱氯化氢并任选通过皂化和再酰化来制备具有式“IMAGE”的化合物,其中R是氢或酰基。 该化合物可用作取代和加成反应的起始原料,并且可用作均聚和共聚中的乙烯基单体,由此形成含有恶唑烷-2-酮环的聚合物。 这些聚合物可用作抗静电剂,染色助剂和离子交换剂。