Abstract:
Compounds of formula I, wherein the substituents R 1 , X, and the index k are as defined in the specification; a process for preparation of compounds of formula I, a process for preparation of its precursor compounds II, wherein the substituents R 1 , X, and the index k are as defined in the specification; intermediates for the production of compounds I, or II; use of compounds of formula I for the production of compounds of formula VI wherein the substituents R 1 , R 3 , and the index k are as defined in the specification; the use of compounds I, or II, for the production of active compounds.
Abstract:
The present invention relates to a process for the preparation of limonene-4-ol by an epoxide ring opening isomerization of terpinolene epoxide.
Abstract:
The present invention relates to a process for providing a compound of formula (IV):wherein R 1 and R 2 are each independently C 1 -C 4 alkyl, and Hal is independently Cl or Br, the process comprising the steps of: (i) reacting a compound of formula (II) wherein R 1 and Hal is defined as above, to obtain a compound of formula (III) wherein R 1 and Hal is defined as above, and (ii) reacting the compound of formula (III) to obtain the compound of formula (IV).
Abstract:
The present invention relates to a process for providing a compound of formula (I): wherein Hal is a halogen, the process comprising the step of: reacting a compound of formula (II) wherein Hal is defined as above, with an alkali metal sulfite of the formula X 2 SO 3 and an alkali metal hydroxide of the formula YOH, wherein X and Y are independently selected from an alkali metal.
Abstract translation:本发明涉及提供式(I)化合物的方法:其中Hal是卤素,该方法包括以下步骤:使其中Hal如上定义的式(II)化合物与碱金属亚硫酸盐反应 的式X 2 SO 3和式YOH的碱金属氢氧化物,其中X和Y独立地选自碱金属。
Abstract:
The present invention relates to a process for manufacturing haloacetamides of formula (I), comprising sub-step (a): reacting halones of formula (II) with oleum; followed by sub-step (b): reacting the reaction mixture obtained in sub-step(a) with an amine of formula (IV) optionally in the presence of a base; wherein the variables are defined according to the description.
Abstract:
The present invention relates to a process for manufacturing fluoroaromatics of formula (I), A-F, comprising step a) diazotization of aminoaromaticsof formula (II) in anhydrous HF with an aqueous solution of a diazotizing agent; followed by step b) thermic decomposition of the diazonium salt of formula (III) resulting from step a); wherein the variables are defined according to the description.
Abstract:
The present invention relates to isothiazoline compounds of formula (I) wherein the variables are as defined in the claims or the description, which are useful for combating or controlling invertebrate pests, in particular arthropod pests and nematodes, and to a method for producing them. The invention also relates to a method for controlling invertebrate pests by using these compounds and to plant propagation material and to an agricultural and a veterinary composition comprising said compounds.
Abstract:
The present invention relates to a process for manufacturing triazinon-benzoxazinones of formula (I), by reacting amino-benzoxazinones of formula (II) with 1,1'-carbonyldiimidazole (CDI) and a (thio)urea compound of formula (III); wherein the variables are defined according to the description.
Abstract:
The present invention relates to a process for manufacturing aryloxyacetamides of formula (I), by reacting haloacetamides of formula (II) with a phenol of formula (III); wherein the variables are defined according to the description, andaryloxyacetamides of formula (I).
Abstract:
The present invention relates to a process for preparing an N-substituted 1 H-pyrazole- 5- carboxylate compound of the formula (l-A) comprising the steps of i) deprotonating a compound of the formula (II) in which the variables R 1 , R 2 and r are each as defined in the description and the claims, with a magnesium-organic base having a carbon bound magnesium; and ii) subjecting the product obtained in step (i) to a carbonylation by reacting it with a reagent selected from the group consisting carbon dioxide or a carbon dioxide equivalent, to obtain a compound of formula (l-A); and it relates to further conversions to yield a N-substituted 1H-pyrazole-5-carbonyl chloride compound of the formula (I).