摘要:
Described herein are intermediate compounds and derivatives thereof that can be synthesized during the preparation of 2,4,5-trifluorophenylacetic acid and derivatives thereof.
摘要:
Useful processes for isolating the fluorinated products formed by reaction with 4-tert-butyl-2,6-dimethylphenylsulfur trifluoride (Fluolead) are disclosed. The processes comprise the conversion of the byproduct (formula I) to sulfinate ester (formula V), and to sulfonate eater (formula VI), and then to the water-soluble sulfonate salt (formula IV) in the presence of the fluorinated products.
摘要:
The present invention relates to a new process for the preparation of 2,4,5-trifluorophenylacetic acid and salts thereof by means of new synthetic intermediates.
摘要:
The invention relates to a process for preparing 2,3,3,3-tetrafluoropropene (CF3CF═CH2), performed using the steps of dehydrohalogenating 1,1,1,2,2-pentafluoropropane (CH3CF2CF3, HFC-245ca) 1,1,1,2-tetrafluoro-2-chloropropane, 1,1,1,2,3-pentafluoropropane (CH2FCHFCF3, HFC-245eb) and/or 1,1,1,2-tetrafluoro-3-chloropropane in the presence of a base, and converting a trifluorodichloropropane or a difluorotrichloropropane or a fluorotetrachloropropane to CH3CF2CF3, 1,1,1,2-tetrafluoro-2-chloropropane, CH2FCHFCF3, and/or 1,1,1,2-tetrafluoro-3-chloropropane.
摘要:
The invention is a method of synthesizing Arylsulfur Trifluorides, such as Fluolead, by reacting BR2 and KF (or suitable alkali metal fluoride) in acetonitrile (or other suitable solvent). The invention also comprises using the Fluolead (or its substitutes), thus prepared, in situ as deoxofluorination reagents with a suitable aldehyde, ketone, or alcohol such as one selected from the group consisting of benzaldehyde Benzaldehyde, p-Bromobenzaldehyde, p-Tolualdehyde, Acetophenone, 2-Butanone, or Isobutyraldehyde, wherein the mixture is heated to reflux until completion. The respective products are then isolated after extraction by hexane and destruction of the sulfinyl fluoride co-product.
摘要:
The present process provides a improved method for the preparation of alkylsulfanyl substituted triazoles 2 which are useful intermediates in a new process for the preparation of triazolones 20.
摘要:
The present process provides a improved method for the preparation of alkylsulfanyl substituted triazoles 2 which are useful intermediates in a new process for the preparation of triazolones 20.
摘要:
Methods and reagents for labeling synthesis of organohalides by transition metal mediated carbonylation reactions using carbon-isotope labeled carbon monoxide are provided. The resultant carbon-isotope labeled organohalides are useful as radiopharmaceuticals, especially for use as precursors in Positron Emission Tomography (PET). Associated PET tracers and kits for PET studies are also provided.
摘要:
The present process provides a improved method for the preparation of alkylsulfanyl substituted triazoles 2 which are useful intermediates in a new process for the preparation of triazolones 20.
摘要:
A layer is spaced between an anode and a cathode and is composed of an organic compound represented by the following general formula [1]. wherein R1 to R10 are each independently a hydrogen atom, a halogen atom, a substituted amino group, an alkyl group, an aryl group, and a heterocyclic group; and X represents (a) an alkylene group having 2 to 6 carbon atoms, wherein in the alkylene group, one or separate two methylene groups may be substituted by —O—, —CO—, —CO—O—, —S—, or —NRa1—, and a hydrogen atom may be substituted by a linear, branched, or cyclic alkyl group having 1 to 10 carbon atoms, (b) an aryl group which may be substituted, or (c) a heterocyclic group which may be substituted, or (d) a fluorine atom.
摘要翻译:一层在阳极和阴极间隔开,由下列通式[1]表示的有机化合物组成。 其中R 1至R 10各自独立地为氢原子,卤素原子,取代的氨基,烷基,芳基和杂环基; X表示(a)具有2〜6个碳原子的亚烷基,其中在亚烷基中,一个或分别的两个亚甲基可以被-O - , - CO - , - CO-O-,-S-, 或-NR a 1 - ,并且氢原子可以被具有1至10个碳原子的直链,支链或环状烷基取代,(b)可以被取代的芳基或( c)可被取代的杂环基,或(d)氟原子。