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Process for the preparation of gamma, delta-unsaturated ketones ba Carroll-reaciton, catalysts for this process and their preparation

机译:γ-卡洛尔反应制得的γ-δ-不饱和酮的方法,该方法的催化剂及其制备方法

摘要

Preparation of gamma , delta -unsaturated ketones (I) by modified Carroll reaction is catalysed by a stable liquid aluminum acetoacetate compound or mixture of such compounds. Some such catalyst mixtures are new. Preparation of gamma , delta -unsaturated ketones of formula (I) involves modified Carroll reaction of an allyl alcohol of formula (II) with diketene or an alkyl acetoacetate of formula (III) in presence of an aluminum catalyst. R1 = H or 1-20C, saturated or unsaturated, branched hydrocarbyl; R2 = 1-5C alkyl. The novelty is that the catalyst consists of an aluminum compound (or aluminum compound mixture) which is a stable liquid at room temperature and contains at least one alkyl acetoacetate-forming group and 1 or 2 alkoxy groups or exclusively alkyl acetoacetate forming groups which are esterified sec. butanol or isobutanol or with at least two different alkanols. Independent claims are included for: (1) new mixtures of aluminum tris-acetoacetates of formula (V) which are liquid at room temperature; and (2) the preparation of mixtures as in (1). R3 = 1-5C alkyl, preferably Me or Et; R4 = 3-10C alkyl, preferably CHMe2, CH(Me)Et, CMe3 or CH(Me)-C3H7; R5 = 1-10C alkyl, preferably Me, Et, CHMe2, CH(Me)Et or CH(Me)-C3H7; provided that R3-R5 are not all the same. A further Independent claim relates to the continuous preparation of compounds (V) (or their mixtures), having the narrower proviso that R3-R5 can only be the same if they are -CH(Me)Et or -CH2CHMe2, which are liquid at room temperature. The process involves continuously reacting 1 mole of aluminum alcoholate of formula (VI) with 3-10 moles of (III), or with at least 3 moles of a mixture of 2 or 3 different compounds (III), optionally dissolved in an inert solvent. Reaction is at 100-250 (preferably 150-200) degrees C and 1-100 (preferably 1-10) bars with a dwell time of 5-120 (preferably 15-45) minutes, the pressure and temperature being such that no gas phase is formed in the reaction vessel. R6 = 2-10C alkyl, preferably -CH2CHMe2, -CH(Me)Et or -CH(Me)C3H7; provided that R2 and R6 can only be the same if they are -CH(Me)Et or -CH2CHMe2.
机译:通过稳定的液态乙酰乙酸铝化合物或此类化合物的混合物催化通过改良的卡洛尔反应制备γ-δ-不饱和酮(I)。一些这样的催化剂混合物是新的。式(I)的γ-δ-不饱和酮的制备涉及在铝催化剂的存在下,式(II)的烯丙醇与式二酮或式(III)的乙酰乙酸烷基酯的改进的卡洛尔反应。 R1 = H或1-20℃,饱和或不饱和的支链烃基; R 2 = 1-5C烷基。新颖之处在于,催化剂由铝化合物(或铝化合物混合物)组成,该铝化合物在室温下为稳定液体,并包含至少一个形成乙酰乙酸烷基酯的基团和1或2个被酯化的烷氧基或仅形成乙酰乙酸烷基酯的基团秒丁醇或异丁醇或至少两种不同的烷醇。包括以下方面的独立权利要求:(1)在室温下为液体的式(V)的三乙酰乙酸铝的新混合物; (2)按照(1)的方法制备混合物。 R3 = 1-5C烷基,优选Me或Et; R4 = 3-10C烷基,优选CHMe2,CH(Me)Et,CMe3或CH(Me)-C3H7; R5 = 1-10C烷基,优选Me,Et,CHMe2,CH(Me)Et或CH(Me)-C3H7;前提是R3-R5不完全相同。另一个独立的权利要求涉及化合物(V)(或其混合物)的连续制备,其具有较窄的条件,即R3-R5仅在它们为-CH(Me)Et或-CH2CHMe2时为相同,它们在-室内温度。该方法包括使1摩尔的式(VI)的铝醇与3-10摩尔的(III),或与至少3摩尔的2或3种不同化合物(III)的混合物连续反应,任选地将其溶于惰性溶剂中。 。反应在100-250(优选150-200)摄氏度和1-100(优选1-10)巴下进行,停留时间为5-120(优选15-45)分钟,压力和温度应确保没有气体在反应容器中形成水相。 R6 = 2-10C烷基,优选-CH2CHMe2,-CH(Me)Et或-CH(Me)C3H7;前提是R2和R6仅在为-CH(Me)Et或-CH2CHMe2时可以相同。

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