In chemistry, dehydrohalogenation is an elimination reaction which removes a hydrogen halide from a substrate. The reaction is usually associated with...

Alkynes are prepared from 1,1- and 1,2-dihaloalkanes by double dehydrohalogenation. The reaction provides a means to generate alkynes from alkenes,...

reacts in a coupling reaction with epichlorohydrin, followed by dehydrohalogenation. Epoxy resins produced from such epoxy monomers are called glycidyl-based...

refrigerant in air conditioners. It is prepared by fluorination and dehydrohalogenation reactions starting with 1,1,1,3,3-pentachloropropane. Cheryl Hogue...

In organic chemistry, an epoxide is a cyclic ether, where the ether forms a three-atom ring: two atoms of carbon and one atom of oxygen. This triangular...

Base-induced bimolecular dehydrohalogenation (an E2 type reaction mechanism). The optimum geometry for the transition state requires the breaking bonds...

as a source of the 2-propenyl group. One early synthesis involves dehydrohalogenation of 1,2-dichloropropane with potassium hydroxide. Takahashi, Tamotsu;...

formation of urethane foams and epoxy resins. It is also useful in dehydrohalogenation reactions and Swern oxidations. Triethylamine is readily alkylated...

is a chemical compound formed by the loss of hydrogen chloride (dehydrohalogenation) from DDT, of which it is one of the more common breakdown products...

which is recycled typically. Sodium amide is a standard base for dehydrohalogenations. It induces the loss of two equivalents of hydrogen bromide from...

n-BuI, which can react with the RLi reagent formed, and by competing dehydrohalogenation reactions, in which n-BuLi serves as a base: 2 C4H9Br + RLi → 2 C4H9R...

triflate). When an alkyl halide is used, the reaction is called a dehydrohalogenation. For unsymmetrical products, the more substituted alkenes (those...

It reacts with C70 and higher fullerenes, but not with C60. As a dehydrohalogenation agent. In surface activation products (primers) for low-surface energy...

chloramine with the formula C5H10NCl. The resulting chloramine undergoes dehydrohalogenation to afford the cyclic imine. 13C NMR: (CDCl3, ppm) 47, 27.2, 25.2[citation...

of trimethylaniline by dibromoethane followed by ring closure and dehydrohalogenation. Nolan, Steven P. (2006). N-Heterocyclic Carbenes in Synthesis. Wiley-VCH...

[Specific proton acceptors as auxiliary bases in alkylation and dehydrohalogenation reactions]. Chemische Berichte (in German). 91 (2). Wiley-VCH: 380–392...

while iodine is the least reactive of them all. The facility of dehydrohalogenation follows the reverse trend: iodine is most easily removed from organic...

well. In the presence of a strong base, alkyl chlorides undergo dehydrohalogenation to give alkenes or alkynes.[citation needed] Alkyl chlorides react...

terminal acetylenes and active methylene compounds. It is useful in dehydrohalogenation reactions. Illustrating the latter behavior, potassium tert-butoxide...

used in situ rather than being isolated. The compound undergoes dehydrohalogenation to afford the cyclic imine. Claxton, George P.; Allen, Lloyd; Grisar...

first obtained by Eugen Bamberger and Wilhelm Lodter in 1893 by dehydrohalogenation of 3-chloro-2-tetralol with hot alkali. 2-Tetralone may be prepared...

brominated, and the resulting dibromodiphenylethane is subjected to dehydrohalogenation. Yet another method involves the coupling of iodobenzene and the...

trichloroethane to give aluminium trichloride, which in turn catalyses the dehydrohalogenation of the remaining trichloroethane to vinylidene chloride and hydrogen...

otherwise it dimerises to biphenylene. Early routes to benzyne involved dehydrohalogenation of aryl halides: Such reactions require strong base and high temperatures...

empirical rule for predicting the favored regiochemistry in the dehydrohalogenation of alkyl iodides, though it turns out that the rule is applicable...

bromination of 1,2-cycloheptanedione with N-bromosuccinimide followed by dehydrohalogenation at elevated temperatures, while another uses acyloin condensation...

diastereoisomer predominates). An example of modest stereoselectivity is the dehydrohalogenation of 2-iodobutane which yields 60% trans-2-butene and 20% cis-2-butene...

at the secondary position, which allows the molecule to undergo dehydrohalogenation easily to give propene, which escapes as a gas and can rupture closed...

dimethylketene. It arises spontaneously when dimethylketene is produced by dehydrohalogenation of isobutyryl chloride with triethylamine. In the presence of aluminium...

magnesium salts and an extended alkyl compound.[citation needed] In dehydrohalogenation reactions, the halogen and an adjacent proton are removed from halocarbons...