Preparation of ionones
    1.
    发明授权
    Preparation of ionones 失效
    紫罗兰酮的制备

    公开(公告)号:US4565894A

    公开(公告)日:1986-01-21

    申请号:US637890

    申请日:1984-08-06

    CPC classification number: C07C403/16 C07C2101/16

    Abstract: Ionones are prepared by cyclization of pseudoionone with concentrated sulfuric acid in the presence of an organic solvent or diluent, while cooling, and by dilution of the reaction mixture with water, by a continuous process in which the pseudoionone is combined with an aliphatic or cycloaliphatic hydrocarbon which boils at 25.degree.-65.degree. C. under the reaction conditions, or an aliphatic chlorohydrocarbon, and the sulfuric acid, with thorough mixing and evaporative cooling by partial or complete vaporization of the solvent present in the reaction mixture, combination being effected so that the temperature of the reaction mixture is from 25.degree. to 65.degree. C. and the residence time of this mixture before it is diluted with water is from 0.5 to 20, preferably from 0.1 to 5, seconds.The novel process can be used to prepare .alpha.- and .beta.-ionone in a technically simple and advantageous manner and in very good yields.

    Abstract translation: 紫罗兰酮是通过在有机溶剂或稀释剂的存在下,用浓硫酸环化来制备的,同时冷却,通过用水稀释反应混合物,其中将假性离子与脂族或脂环族烃结合 在反应条件下在25°-65℃下沸腾,或在脂肪族氯代烃和硫酸中,通过部分或完全蒸发存在于反应混合物中的溶剂进行充分混合和蒸发冷却,进行组合,使得 反应混合物的温度为25-65℃,该混合物在用水稀释之前的停留时间为0.5-20秒,优选为0.1-5秒。 该新方法可用于以技术上简单和有利的方式以非常好的产率制备α-和β-丁酮。

    Increasing the yield of 2.5.6-trimethylcyclohex-2-en-1-one
    2.
    发明授权
    Increasing the yield of 2.5.6-trimethylcyclohex-2-en-1-one 失效
    提高2.5.6-三甲基环己-2-烯-1-酮的产率

    公开(公告)号:US4820874A

    公开(公告)日:1989-04-11

    申请号:US111603

    申请日:1987-10-23

    CPC classification number: C07C49/603 C07C45/74 C07C45/78 C07C45/82 C07C45/85

    Abstract: The yield of 2,5,6-trimethyl-cyclohex-2-en-1-one is increased by reacting diethyl ketyone, in the presence of an alkali, with crotonaldehyde or a compound which is converted to crotonaldehyde under the reaction conditions chose, and working up the reaction mixture by distillation, by a method in which the distillation residue obtained is either(a) heated at from 120.degree. to 250.degree. C. in particular from 120.degree. to 200.degree. C., with the addition of a catalytic amount of an alkali, or(b) heated at from 150.degree. to 250.degree. C. without the addition of such a substance,and the mixture of 2,5,6-trimethylcyclohex-2-en-1-one and diethyl ketone which is formed from the distillation residue as a result of the heat treatment is separated by distillation.

    Abstract translation: 在碱存在下,使二乙基酮与巴豆醛或在选择的反应条件下转化为巴豆醛的化合物反应,使2,5,6-三甲基 - 环己-2-烯-1-酮的产率增加, 并通过蒸馏处理反应混合物,通过其中所得蒸馏残余物(a)在120℃至250℃,特别是120℃至200℃加热的方法,加入催化剂 碱的量,或(b)在不加入这种物质的情况下在150-250℃下加热,以及2,5,6-三甲基环己-2-烯-1-酮和二乙基酮的混合物,其中 由蒸馏残渣形成的热处理结果通过蒸馏分离。

    Preparation of higher unsaturated ketones
    3.
    发明授权
    Preparation of higher unsaturated ketones 失效
    制备较高级的不饱和酮

    公开(公告)号:US4310705A

    公开(公告)日:1982-01-12

    申请号:US163401

    申请日:1980-06-26

    CPC classification number: C07C45/676

    Abstract: An improved process for the preparation of higher unsaturated ketones, such as geranylacetone and farnesylacetone, by reacting a .beta.,.gamma.-unsaturated alcohol and an alkyl acetoacetate at an elevated temperature in the presence of an organic aluminum compound, with elimination, and removal, of the alcohol derived from the alkyl acetoacetate in a reactor system carrying a fractionating column. The improvement in the purity, yield, and especially space-time yield of the product is achieved by starting from an alcohol having a higher boiling point than that of the alkyl acetoacetate used, carrying out the reaction in the presence of a small amount of an inert liquid which has a boiling point between that of the alkyl acetoacetate and the alcohol to be eliminated therefrom, and ensuring that the temperature at the bottom of the fractionating column is only slightly higher than the boiling point of the added liquid, under the prevailing pressure.

    Abstract translation: 通过在有机铝化合物的存在下在升高的温度下使β,γ-不饱和醇和乙酰乙酸烷基酯反应来制备高级不饱和酮,如香叶基丙酮和法呢基丙酮的改进方法,消除和除去 在含有分馏塔的反应器系统中衍生自乙酰乙酸烷基酯的醇。 通过从具有比所用乙酰乙酸烷基酯的沸点高的醇开始的醇开始,在少量的存在下进行反应来实现产物的纯度,产率和特别的时空产率的改善 沸点在乙酰乙酸烷基酯和被除去的醇之间的沸点的惰性液体,并且确保分馏塔底部的温度仅略高于添加液体的沸点,在主要压力下 。

    Efficient method of decoupling the downloading of a memory map and execution of a utility program contained in the memory map
    4.
    发明授权
    Efficient method of decoupling the downloading of a memory map and execution of a utility program contained in the memory map 有权
    解除存储器映射的下载和存储器映射中包含的实用程序的有效方法

    公开(公告)号:US09405559B2

    公开(公告)日:2016-08-02

    申请号:US13811513

    申请日:2011-05-27

    CPC classification number: G06F9/445 G06F8/65 Y02D10/42

    Abstract: A method of executing a utility program on a computer system having a system management chip includes activating a graphics memory in the computer system, downloading a memory map including the utility program to be executed by the system management chip, storing the memory map in the graphics memory by the system management chip, copying the memory map from the graphics memory to a main memory in the computer system, and executing the utility program with a processor in the computer system.

    Abstract translation: 一种在具有系统管理芯片的计算机系统上执行应用程序的方法,包括激活计算机系统中的图形存储器,下载包括由系统管理芯片执行的应用程序的存储器映射,将存储器映射存储在图形中 通过系统管理芯片的存储器,将存储器映射从图形存储器复制到计算机系统中的主存储器,以及在计算机系统中用处理器执行实用程序。

    METHOD FOR EXECUTING A UTILITY PROGRAM, COMPUTER SYSTEM AND COMPUTER PROGRAM PRODUCT
    5.
    发明申请
    METHOD FOR EXECUTING A UTILITY PROGRAM, COMPUTER SYSTEM AND COMPUTER PROGRAM PRODUCT 有权
    执行实用程序,计算机系统和计算机程序产品的方法

    公开(公告)号:US20130219398A1

    公开(公告)日:2013-08-22

    申请号:US13811513

    申请日:2011-05-27

    CPC classification number: G06F9/445 G06F8/65 Y02D10/42

    Abstract: A method of executing a utility program on a computer system having a system management chip includes activating a graphics memory in the computer system, downloading a memory map including the utility program to be executed by the system management chip, storing the memory map in the graphics memory by the system management chip, copying the memory map from the graphics memory to a main memory in the computer system, and executing the utility program with a processor in the computer system.

    Abstract translation: 一种在具有系统管理芯片的计算机系统上执行应用程序的方法,包括激活计算机系统中的图形存储器,下载包括由系统管理芯片执行的应用程序的存储器映射,将存储器映射存储在图形中 通过系统管理芯片的存储器,将存储器映射从图形存储器复制到计算机系统中的主存储器,以及在计算机系统中用处理器执行实用程序。

    Preparation of polyunsaturated ketones
    8.
    发明授权
    Preparation of polyunsaturated ketones 失效
    多不饱和酮的制备

    公开(公告)号:US4431844A

    公开(公告)日:1984-02-14

    申请号:US361249

    申请日:1982-03-24

    CPC classification number: C07C49/203 C07C45/74

    Abstract: An improved process for the preparation of unsaturated ketones of the general formula I ##STR1## where R.sup.1 is --CH.sub.3, ##STR2## and R.sup.2 and R.sup.3 are different and each is H or --CH.sub.3, by reacting an aldehyde of the general formula II ##STR3## with a molar excess of acetone or methyl ethyl ketone at an elevated temperature in the presence of an aqueous alkali metal hydroxide solution, wherein (a) all the reactants are mixed thoroughly, (b) the temperature is kept at from 10 to 120.degree. C. above the boiling point of the lowest-boiling component and (c) the pressure is kept at from p to 100 bar, where p is the vapor pressure of the mixture at the reaction temperature.The products methylpseudoionone, dimethylpseudoionone, pseudoirone, methylpseudoirone and dimethylpseudoirone are useful scents and scent intermediates. In addition, pseudoionone is an important intermediate for the industrial preparation of vitamin A, and 6-methyl-hepta-3,5-dien-2-one is a sought-after aromatic.

    Abstract translation: 制备通式I(I)的不饱和酮的改进方法,其中R 1为-CH 3,R 2和R 3不同,各自为H或-CH 3,通式 在碱金属氢氧化物水溶液的存在下,在升高的温度下用摩尔过量的丙酮或甲基乙基酮制备式II(II)化合物,其中(a)所有反应物充分混合,(b)温度为 保持在最低沸点组分的沸点以上10至120℃,和(c)压力保持在p至100巴,其中p是反应温度下混合物的蒸气压。 产物甲基假ion酮,二甲基假ion酮,假呋酮,甲基假酮和二甲基假酮是有用的香味和香味中间体。 此外,假雄酮是维生素A工业制备的重要中间体,6-甲基 - 庚-3,5-二烯-2-酮是一种追求的芳香族。

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