首页> 外国专利> 2 - Exo - hydroxy - endo - tricyclo (6.2.1.0 (arrow high) 2 (arrow high) (arrow high), (arrow high) (arrow high) 7 (arrow high)) undecane

2 - Exo - hydroxy - endo - tricyclo (6.2.1.0 (arrow high) 2 (arrow high) (arrow high), (arrow high) (arrow high) 7 (arrow high)) undecane

机译:2-外-羟基-内-三环(6.2.1.0(箭头高)2(箭头高),(箭头高)(箭头高)7(箭头高))十一烷

摘要

NEW MATERIAL:2-Exo-hydroxy-endo-tricyclo[6.2.1.02.7]undecane of formula I . USE:Perfume. It has strong green, camphor-like, or woody fragrance similar to a component of patchouli oil, and is useful for the control of the perfume of lavender-type, lavandine-type, bergamot-type, fusea-type and sypre-type. Since the compound has a polycyclic aliphatic structure similar to natural sesquiterpene alcohols, the compound is expected to have pharmacological activities such as antiviral, antibacterial and plant-hormone activities. PREPARATION:The compound of formula I is produced by reacting 1mol of endo-tricyclo[6.2.1.02.7]undecane of formula II with 1-10mol of a peracid such as m-chloroperbenzoic acid in a solvent such as 1,2-dichloroethane for 5-40hr under refluxing, thereby hydroxylating the bridge-top of the starting compound.
机译:新材料:式I的2-外-羟基-内-三环[6.2.1.0 <2.7>]十一烷。用途:香水。它具有类似于广oul香油成分的强烈的绿色,樟脑样或木质香气,可用于控制薰衣草型,薰衣草型,佛手柑型,fuse香型和丁香型的香水。由于该化合物具有类似于天然倍半萜烯醇的多环脂族结构,因此预期该化合物具有药理活性,例如抗病毒,抗菌和植物激素活性。制备:式I的化合物是通过使1摩尔的式II的三环内[6.2.1.0 2.7]十一碳十一烷与1-10摩尔的过酸,例如间氯过苯甲酸,在1,2-的溶剂中反应而制得的。在回流下于二氯乙烷中反应5-40小时,从而使起始化合物的桥顶羟基化。

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