the reduction of aromatic and olefinic compounds with lithium or calcium to unsaturated the Benkeser reduction,6 the Benkeser reduction in ethylenediamine. Benkeser Reduction R. A. Benkeser et al., J. Am. Chem. Soc. 74, (); 77 , (). Reduction of aromatic and olefinic compounds with lithium or. Notes- Benkeser Reduction of Norbornadiene and Norbornene. James Traynham. J. Org. Chem., , 25 (5), pp – DOI: /joa

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Journal of the Chemical Society, Perkin Transactions 1. Fetching data from CrossRef. The Benkeser Reduction Reaction. It is miscible with virtually all solvents. Purified trichlorosilane is the principal precursor to ultrapure silicon in the semiconductor industry.

If you are the author of this article you do not need to formally request permission to reproduce figures, diagrams etc. In water, it rapidly decomposes to produce a silicone polymer while giving off hydrochloric acid. Member feedback about List of organic reactions: Well-known reactions and reagents in organic chemistry include 1,3-Dipolar cycloaddition 2,3-Wittig rearrangement A Abramovitch—Shapiro tryptamine synthesis Acetalisation Acetoacetic ester condensation Achmatowicz reaction Acylation Acyloin condensation Adams catalyst Adams decarboxylation Adkins catalyst Adkins—Peterson reaction Akabori amino acid reaction Alcohol oxidation Alder ene reaction Alder—Stein rules Aldol addition Aldol condensation Algar—Flynn—Oyamada reaction Alkylimino-de-oxo-bisubstitution Alkyne trimerisation Alkyne zipper reaction Allan—Robinson reaction Allylic rearrangement Amadori rearrangement Amine alkylation Angeli—Rimini reaction Andrussov oxidation Appel reaction Arbuzov reaction, Arbusow reaction Arens—van Dorp synthesis, Isler modification Aromatic nitration Arndt—Eistert synthesis Auwers synthesis Azo coupling B Baeyer—Drewson indigo synthesis Baeyer—Villiger oxidation Baeyer—Villiger rearrangement Bakeland process Bakelite Reduction of five aryltrimethylsilanes and one cyclohexenyltrimethylsilane with lithium in ethylamine gives cyclohexanes in every case.


Benkeser reaction | Revolvy

Authors contributing to RSC publications journal reductiob, books or book chapters do not need to formally request permission to reproduce material rsduction in this article provided that the correct acknowledgement is given with the reproduced material. Wilds later discovered that lithium gives better yields. For the reduction naphthalene with lithium in a mixed ethylamine – dimethylamine solution, the principal products are bicyclo[3. Cleavage of one carbon—silicon bond occurs in 1,3-bis trimethylsilyl benzene and 1,3,5-tris trimethylsilyl benzene.

Back to tab navigation. For reproduction of material from NJC: Member feedback about Ethylamine: Reduction of aryltrimethylsilanes as a synthetic method. Member feedback about Trichlorosilane: Back to tab navigation Fetching data from CrossRef.

XX is the XXth reference in the list of references. Hydrogen is also produced, as described in the chemical equation: Member feedback about Birch reduction: It is a colourless, volatile bemkeser. The reaction was reported in by the Australian chemist Arthur Birch — working in the Dyson Perrins Laboratory at the University of Oxford,[1][2][3][4][5][6] building on earlier work by Wooster and Godfrey published in The original reaction reported by Arthur Birch in used sodium and ethanol.

Ethylamines Revolvy Brain revolvybrain.

It is also produced from silicon tetrachloride: For reproduction of material from PCCP: The major byproducts are silicon tetrachloride chemical formula SiClhexachlorodisilane SiCland dichlorosilane HSiClfrom which trichlorosilane can be separated by distillation. You do not have JavaScript enabled. This reaction is quite unlike catalytic hydrogenation, which usually reduces the aromatic ring all the way to a cyclohexane.


This colourless gas has a strong ammonia-like odor.

Benkeser reaction – Wikipedia

Search articles by author Colin Eaborn. The Birch reduction is an organic reaction which is particularly useful in synthetic organic chemistry. If you are not the author of this article and you wish to reproduce material from it in a third party non-RSC publication you must formally request rwduction using Copyright Clearance Center.

Trichlorosilane topic Trichlorosilane is an inorganic compound with the formula HSiCl. If you are the author of this article you still need to obtain permission to reproduce the whole article in a third party publication with the exception of reproduction of the whole article in a thesis or dissertation.

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This reaction is a modification of the Birch reductionwhere ammonia is the solvent. Kaiser and Robert A. For reproduction of material from PPS: Birch reduction topic The Birch reduction is an organic reaction which is particularly useful in synthetic reducttion chemistry. The reaction is wi In all cases the Ref.