Abstract:
The present invention relates to a process for the preparation of fluoromethyl-substituted heterocyclic compounds of the general formula (I), in which R1 is H or F; R2 is a group -[A-O]m-R3, in which A is C2-C4-alkanediyl, R3 is C1-C4-alkyl and m is 1 or 2, by reaction of the corresponding chloromethyl-substituted compounds (II) in the presence of fluorinating agents, to processes for preparing the chloromethyl-substituted compounds (II), to processes for preparing amides of the general formula (IV), and to compounds of the general formulae (I) and (II).
Abstract:
The invention relates to heteroaroyl-substituted alanines of formula (I), in which the variables A and R1 to R8 are defined as cited in the description, and to their agriculturally useful salts. The invention also relates to methods and intermediates for producing said compounds, to the use of said compounds or to agents containing the latter for controlling undesirable plants.
Abstract:
Pesticidal compositions comprising 3-pyridyl derivatives of formula (I) and/or formula (II) wherein the variables and indices are as defined in the description, and an agronomically acceptable carrier, processes for the preparation of compounds I and use of compounds I or II and the compositions comprising them for combating pests.
Abstract:
The present invention relates to a process for providing a compound of formula (I):, wherein R is hydrogen or R', wherein R' is –(C1-C4)alkyl, and 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 alkoxide of the formula XOR', wherein X is an alkali metal, and R' is defined as above.
Abstract:
The present invention relates to a process for providing a compound of formula (I):, wherein R is hydrogen or R', wherein R' is –(C1-C4)alkyl, and 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 alkoxide of the formula XOR', wherein X is an alkali metal, and R' is defined as above.
Abstract:
The present invention relates to a process for manufacturing 4-propargylated amino- benzoxazinones of formula (I), comprising the following steps: step a) preparing propargyl chloride by reacting propargyl alcohol with thionyl chloride optionally in the presence of a catalyst; and step b) reacting the propargyl chloride prepared in step (a) with a NH-benzoxazinone of formula (II); wherein the variables are defined according to the description.
Abstract:
The present invention relates to carbamat-benzoxazinones of formula (I), wherein the variables are defined according to the description, 5 as well as to a process for manufacturing carbamat-benzoxazinones of formula (I), and to the use of carbamat-benzoxazinones of formula (I) in manufacturing benzoxazinones of formula (X).