Electrophilic bromination of alkenes: environmental, health and safety aspects of new alternative methods.

Chemistry

Gymnasium Ganderkesee, Am Steinacker 12, 27777 Ganderkesee, Germany.

Published: February 2009

More than twenty new alternative methods for bromination of alkenes have been evaluated taking into consideration their resource demands, waste production as well as environmental, health and safety aspects. The cost of bromine and the substances designated to circumvent the application of molecular bromine have also been taken into account. As bromine is only one of several problematic substances being used, its avoidance-by applying bromine supported on solid material or by performing the in situ generation of bromine-does not significantly reduce the technological requirements. On the contrary, the resource demands and amount of waste produced by most new methods are significantly higher compared to the standard methods, especially if the recycling of a carrying agent is not efficient. The method using hydrobromic acid and hydrogen peroxide can be regarded as a competitive alternative to the standard method. The application of certain carrying agents could be interesting, because solvents such as carbon tetrachloride or chloroform used during synthesis could be replaced with less problematic ones during work-up. However, problems associated with these alternatives are not resolved as yet.

Download full-text PDF

Source
http://dx.doi.org/10.1002/chem.200800462DOI Listing

Publication Analysis

Top Keywords

bromination alkenes
8
environmental health
8
health safety
8
safety aspects
8
alternative methods
8
resource demands
8
electrophilic bromination
4
alkenes environmental
4
aspects alternative
4
methods
4

Similar Publications

Most molecular catalysts have been developed employing polar functional groups as catalytic sites. However, the use of non-polar functional groups for catalysis has received less attention due to their modest molecular interactions while the bioorthogonal reactivity of non-polar alkenes as substrates is frequently used in click chemistry. In this study, we conducted mechanistic studies on the catalysis of trans-cyclooctene (TCO) derivatives with the strained olefin as the catalytic site using kinetic and computational analyses to aid the design of more active olefin catalysts.

View Article and Find Full Text PDF

Pyrometallurgy has proven to be a highly effective method for the large-scale recycling of waste printed circuit boards (WPCB) in industrial settings. This study focused on the fast pyrolysis characteristics of WPCB at smelting temperatures and characterized the gas product release behavior and solid product features in detail. The results indicate that the pyrolysis gas was mainly composed of H, CH and CO, and the maximum yield of pyrolysis gas was obtained at 1300 °C, which was 233.

View Article and Find Full Text PDF
Article Synopsis
  • The chemistry of hypervalent iodine (HVI) reagents is gaining popularity for synthesizing various chemical structures due to their unique reactivity as oxidants and electrophiles.
  • HVI reagents are affordable, non-toxic, and environmentally friendly, making them appealing for chemical synthesis.
  • A key application is the intramolecular HVI-mediated halocyclisation of alkenes, utilizing different nucleophiles (like carbon, oxygen, nitrogen, or sulfur) to create halogenated cyclic compounds, with literature examples categorized by the halogens and nucleophiles used.
View Article and Find Full Text PDF

Herein, we demonstrate a practical dual ligand-enabled iron photocatalysis paradigm-converting all kinds of halogen-containing carboxylates (C X COO, X: F, Cl, Br) into C X radicals for the valuable chloro/fluoro-polyhaloalkylation of non-activated alkenes with easily available trichloroacetonitrile/Selectfluor as the electrophilic halogenation reagent. The modular assembly of the effective iron and C X COO-based light-harvesting species using the two ligands-OMe/CF-substituted bipyridine and acetonitrile/trichloroacetonitrile is evidenced by detailed mechanistic studies. The late-stage modification, low loading amount of iron (TON: 257) and feasible gram-scale synthesis show the utility of this protocol.

View Article and Find Full Text PDF

The stereochemistry of the uncatalyzed chlorolactonization of 4-phenylpent-4-enoic acid at room temperature was examined to probe the reaction's intrinsic diastereoselectivities as a function of chlorenium ion donor, solvent polarity, and reactant concentration ranges. Kinetic studies using Variable Time Normalization Analysis (VTNA) revealed differing reaction orders for the syn and anti alkene addition processes. Aided and illustrated by quantum chemical modeling, this detailed mechanistic analysis of the substrate's intrinsic chlorolactonization reactions points to concerted Ad3-type paths for both syn and anti additions.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!