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    • 3. 发明授权
    • Preparation of C10-C30-alkenes by partial hydrogenation of alkynes over fixed-bed supported palladium catalysts
    • 通过固定床负载的钯催化剂上的炔进行部分氢化制备C10-C30-烯烃
    • US06365790B2
    • 2002-04-02
    • US09734024
    • 2000-12-12
    • Klaus ReimerGerd KaibelUlrich KammelFranz Josef BröckerAndreas AnsmannHeinz EtzrodtManfred StroezelMathias HaakeLothar LaupichlerBernhard Bockstiegel
    • Klaus ReimerGerd KaibelUlrich KammelFranz Josef BröckerAndreas AnsmannHeinz EtzrodtManfred StroezelMathias HaakeLothar LaupichlerBernhard Bockstiegel
    • C07C2900
    • C07C29/17B01J23/44B01J23/50B01J35/04B01J35/06B01J37/0217B01J37/0225B01J37/08C07C5/09C07C2523/44C07C11/02C07C33/025C07C33/02
    • Alkenes are prepared by partial hydrogenation of alkynes in the liquid phase at from 20 to 250° C. and hydrogen partial pressures of from 0.3 to 200 bar over fixed-bed supported palladium catalysts which are obtainable by heating the support material in the air, cooling, applying a palladium compound and, if required, additionally other metal ions for doping purposes, molding and processing to give monolithic catalyst elements, by a process in which A) alkynes of 10 to 30 carbon atoms are used as starting compounds, B) the palladium compound and, if required, the other metal ions are applied to the support material by impregnation of the heated and cooled support material with a solution containing palladium salts and, if required, other metal ions and subsequent drying, and C) from 10 to 2000 ppm of carbon monoxide (CO) are added to the hydrogenation gas or a corresponding amount of CO is allowed to form in the liquid phase by slight decomposition of a compound which is added to the reaction mixture and eliminates CO under the reaction conditions. The process is particularly advantageous if the partial hydrogenation is carried out in a tube reactor by the trickle-bed or liquid phase procedure with product recycling at cross-sectional loadings of from 20 to 500 m3/m2*h. The process is particularly suitable for the preparation of 3,7,11,15-tetramethyl-1-hexadecen-3-ol (isophytol), 3,7,11-trimethyl-l-dodecen-3-ol (tetrahydronerolidol), 3,7,11-trimethyl-1,4-dodecadien-3-ol, 3,7,11-trimethyl-1,6-dodecadien-3-ol (dihydronerolidol), 3,7-dimethyloct-1,6-dien-3-ol or 3,7-dimethyloct-1-en-3-ol from the corresponding alkynes.
    • 烯烃通过液相中炔烃在20至250℃的部分氢化和固定床负载的钯催化剂的0.3至200巴的氢分压来制备,其可通过加热空气中的载体材料,冷却 使用钯化合物,另外还需要另外的金属离子用于掺杂目的,通过使用10-30个碳原子的炔烃作为起始化合物的方法,模塑和加工以得到整体式催化剂元素,B)钯 如果需要,另外的金属离子通过用含有钯盐的溶液浸渍加热和冷却的载体材料以及如果需要的话其它金属离子并随后干燥而被施加到载体材料上,C)为10-2000ppm 的一氧化碳(CO)加入到氢化气体中,或者相应量的CO在液相中形成,通过轻微分解添加到真空中的化合物 并且在反应条件下消除CO。如果部分氢化在管式反应器中通过滴流床或液相方法进行,则该方法是特别有利的,其中产物回收的横截面负荷为20-500m 3 / m2 * h。 该方法特别适用于制备3,7,11,15-四甲基-1-十六碳烯-3-醇(异山梨糖醇),3,7,11-三甲基-1-十二碳烯-3-醇(四氢化吗啉醇),3 ,7,11-三甲基-1,4-十二碳二烯-3-醇,3,7,11-三甲基-1,6-十二碳二烯-3-醇(二氢吗啉醇),3,7-二甲基辛-1,6-二烯 - 3-醇或3,7-二甲基辛-1-烯-3-醇。
    • 10. 发明授权
    • Process for preparing ionones
    • 紫罗兰酮的制备方法
    • US06288282B1
    • 2001-09-11
    • US09567268
    • 2000-05-09
    • Udo RheudeUlrich HörcherDietmar WellerManfred Stroezel
    • Udo RheudeUlrich HörcherDietmar WellerManfred Stroezel
    • C07C4921
    • C07C403/16C07C2601/16
    • Process for the continuous preparation of &agr;- and/or &bgr;-ionone or homologous compounds using concentrated sulfuric acid at temperatures from 20 to 90° C., in the presence of organic solvents or diluents with cooling and by subsequent termination of the reaction by hydrolysis of the reaction mixture with water or dilute sulfuric acid, wherein both the cyclization of pseudoionones and the subsequent hydrolysis of the reaction mixture are carried out in a virtually adiabatic reaction in one or more reaction mixing pump(s) which are connected in series and each of which consists essentially of a rotationally symmetrical mixing chamber formed from a peripheral wall and two end walls and of a mixing rotor made of material inert to sulfuric acid and with rotational drive, where the mixing chamber has at least one inlet opening for each component and one outlet opening for the reaction mixture, and annular channels in fluid connection to one another in the end walls, and wherein the heat of the two reactions is in each case partly or wholly removed with the aid of a downstream heat exchanger.
    • 使用浓硫酸在20〜90℃的温度下,在有机溶剂或稀释剂存在下,在冷却下,随后通过水解终止反应,连续制备α-和/或β-紫罗兰酮或同系化合物的方法 反应混合物与水或稀硫酸反应,其中假戊烯酮的环化和随后的反应混合物的水解在一个或多个反应混合泵中实质上绝热的反应中进行,所述反应混合泵串联连接, 其基本上由旋转对称的混合室组成,该混合室由周壁和两个端壁以及由硫酸惰性且具有旋转驱动的材料制成的混合转子,其中混合室具有用于每个部件的至少一个入口, 用于反应混合物的一个出口,以及在端壁中彼此流体连接的环形通道,其中热量 在每种情况下,两个反应在下游热交换器的帮助下部分或全部去除。