134932-08-4

Basic information

• Product Name: (1R,2Ξ)-1,2-dimethyl-cyclopentane
• CAS NO: 134932-08-4
• Molecular Weight: 98.1882
• Mol File: 134932-08-4.mol

Chemical Properties

• CAS DataBase Reference: (1R,2Ξ)-1,2-dimethyl-cyclopentane(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2Ξ)-1,2-dimethyl-cyclopentane(134932-08-4)
• EPA Substance Registry System: (1R,2Ξ)-1,2-dimethyl-cyclopentane(134932-08-4)

Safety Data

• Hazardous Substances Data: 134932-08-4(Hazardous Substances Data)

Upstream product

• 765-47-9 1,2-dimethylcyclopentene 
• 58049-91-5 3,3-dimethylcyclopentene 
• 142-82-5 n-heptane 
• 3070-53-9 1,6-heptadiene 
• 112-17-4 n-decyl acetate 
• 15661-92-4 1-methyl-5-hexenyl chloride 
• 13389-36-1 6-iodohept-1-ene 
• 38334-98-4 6-bromo-1-heptene 
• 108-88-3 toluene 
• 7446-70-0 aluminium trichloride 
• 82166-21-0 methyl cyclohexane 
• 64-19-7 acetic acid 
• 589-34-4 3-methyl-hexane 
• 10034-85-2 hydrogen iodide 

Downstream Products

• 13505-34-5 2,6-heptandione 

Relevant articles and documents

Catalytic cycloisomerization of unsaturated organoiodides

Catalytic quantities of phenyllithium (PhLi) have been found to initiate novel 5-exo cycloisomerization of a variety of structurally diverse unsaturated organoiodides. The isomerization reaction appears to be a process of broad synthetic utility for the preparation of iodomethyl-substituted five-membered rings. Primary, secondary, tertiary, or aryl iodides tethered to a suitably positioned carbon-carbon π-bond are converted cleanly to their cyclic isomers in good to excellent yield (i.e., 70-90%) by simply allowing a hydrocarbon-MTBE solution of the iodide to stand in the presence of a small quantity of PhLi at an appropriate temperature. The mechanism of the cycloisomerization was found to be substrate dependent: unsaturated aryl and primary alkyl iodides undergo isomerization via a three-step cascades (eqs 1- 3) mediated by two reversible lithium-iodine exchange reactions bracketing an irreversible 5-exo cyclization of an unsaturated organolithium; unsaturated secondary and tertiary alkyl iodides apparently isomerize via a radical- mediated atom transfer process initiated by homolytic fragmentation of the ate-complex generated upon attack of PhLi on the iodine atom of the substrate.

Insights into the Major Reaction Pathways of Vapor-Phase Hydrodeoxygenation of m-Cresol on a Pt/HBeta Catalyst

Conversion of m-cresol was studied on a Pt/HBeta catalyst at 225-350°C and ambient hydrogen pressure. At 250°C, the reaction proceeds through two major reaction pathways: (1) direct deoxygenation to toluene (DDO path); (2) hydrogenation of m-cresol to methylcyclohexanone and methylcyclohexanol on Pt, followed by fast dehydration on Br?nsted acid sites (BAS) to methylcyclohexene, which is either hydrogenated to methylcyclohexane on Pt or ring-contracted to dimethylcyclopentanes and ethylcyclopentane on BAS (HYD path). The initial hydrogenation is the rate-determining step of the HYD path as its rate is significantly lower than those of subsequent steps. The apparent activation energy of the DDO path is 49.7 kJ mol-1 but the activation energy is negative for the HYD path. Therefore, higher temperatures lead to the DDO path becoming the dominant path to toluene, whereas the HYD path, followed by fast equilibration to toluene, is less dominant, owing to the inhibition of the initial hydrogenation of m-cresol.

Synthesis, reactivity, and catalytic application of a nickel pincer hydride complex

The nickel(II) hydride complex [(MeN2N)Ni-H] (2) was synthesized by the reaction of [(MeN2N)Ni-OMe] (6) with Ph2SiH2 and was characterized by NMR and IR spectroscopy as well as X-ray crystallography. 2 was unstable in solution, and it decomposed via two reaction pathways. The first pathway was intramolecular N-H reductive elimination to give MeN2NH and nickel particles. The second pathway was intermolecular, with H2, nickel particles, and a five-coordinate Ni(II) complex [(MeN2N)2Ni] (8) as the products. 2 reacted with acetone and ethylene, forming [( MeN2N)Ni-OiPr] (9) and [(MeN 2N)Ni-Et] (10), respectively. 2 also reacted with alkyl halides, yielding nickel halide complexes and alkanes. The reduction of alkyl halides was rendered catalytically, using [(MeN2N)Ni-Cl] (1) as catalyst, NaOiPr or NaOMe as base, and Ph2SiH2 or Me(EtO)2SiH as the hydride source. The catalysis appears to operate via a radical mechanism.

Study of Ir/WO3/ZrO2-SiO2 ring-opening catalysts: Part II. Reaction network, kinetic studies and structure-activity correlation

The present paper is the second part of a systematic study of the influence of W and Ir loading on the activity of Ir/WO3/ZrO2-SiO2 catalysts for the ring-opening reaction of naphthenic molecules using methylcyclohexane (MCH) as a model compound. A series of Si-stabilized tungstated zirconias, WOx/ZrO2-SiO2, containing up to 3.5 atom W/nm2, was prepared. Ir-based catalysts containing up to 1.2 wt% were obtained by impregnation of these solids. Characterization of the metal dispersion and catalyst acidity was described in a previous article. The objective of the present study was to determine the best metal/acid balance for optimal performance of Ir/WOx/ZrO2-SiO2 catalysts in the ring-opening reaction of MCH. Monofunctional (acid WOx/ZrO2-SiO2 or metal Ir/ZrO2-SiO2) and bifunctional (Ir/WO3/ZrO2-SiO2) catalysts were examined. Based on the analysis of the yields and products distributions, a reaction network was proposed, and kinetic data (e.g., activation energies, initial rates) were calculated. Correlations between characterization results obtained earlier (e.g., acidity, dispersion) and catalytic performance are also reported. The monofunctional acid catalysts WOx/ZrO2-SiO2 showed a low selectivity for ring opening. The ring-contraction activity developed for W surface density above a threshold value of 1 atom W/nm2. This was attributed to the appearance and the development of a relatively strong Broensted acidity monitored by infrared measurements. MCH ring contraction and C5 naphthene ring opening occur according to a classic acid mechanism. For low conversions, the monofunctional metal catalysts Ir/ZrO2-SiO2 exhibited significant selectivity for ring opening that decreased with increasing conversion. Because of the lack of ring-contraction products, the observed activity was attributed to the direct ring opening of the MCH. Ring opening and cracking occur according to a dicarbene mechanism. The study of MCH conversion on Ir/WOx/ZrO2-SiO2 catalysts indicated that MCH ring contraction to alkylcyclopentanes occurs before ring opening. The best yields for ring opening were obtained with the 1.2% Ir/WOx/ZrO2 (1.5 atom of W/nm2). Further increases in W surface density led to a decrease in the indirect ring-opening yield, attributed to a decrease in Ir dispersion. For bifunctional metal/acid catalysts, analysis of the mechanism is less straightforward. The activation energy for C6 ring contraction and indirect C6 ring opening is a function of the metal/acid ratio. For high ratios, indirect ring opening occurs essentially over metallic sites. A decrease in the metal/acid ratio enhances the contribution of acid mechanism.

Avoiding olefin isomerization during decyanation of alkylcyano α,ω-dienes: A deuterium labeling and structural study of mechanism

(Chemical Equation Presented) A two-step synthetic pathway involving decyanation chemistry for the synthesis of pure alkyl α,ω-dienes in quantitative yields is presented. Prior methodologies for the preparation of such compounds required 6-9 steps, sometimes leading to product mixtures resulting from olefin isomerization chemistry. This isomerization chemistry has been eliminated. Deuteration labeling and structural mechanistic investigations were completed to decipher this chemistry. Deuterium labeling experiments reveal the precise nature of this radical decyanation chemistry, where an alcohol plays the role of hydrogen donor. The correct molecular design to avoid competing intramolecular cyclization, and the necessary reaction conditions to avoid olefin isomerization during the decyanation process are reported herein.

A novel reduction of polycarboxylic acids into their corresponding alkanes using n-butylsilane or diethylsilane as the reducing agent

A convenient one-pot reaction has been developed for the reduction of polycarboxylic acids on aliphatic and aromatic systems to their corresponding alkanes. The reduction utilises either diethylsilane or n-butylsilane as the reducing agent in the presence of the Lewis acid catalyst tris(pentafluorophenyl)borane.

Pyrolysis of Alkyl Acetates. A Radical Pathway for the Formation of Minor Products

Decyl acetate and decene pyrolysis under the same reaction conditions show that the formation of the minor products during the pyrolysis of esters occurs by a parallel, and not a secondary, reaction.The radioactivity observed in the CO2 and CO produced during the pyrolysis of 1-hexyl acetate-1-14C and the radioactivity in the methane from the pyrolysis of 1-hexyl acetate-2-14C strongly suggested a radical reaction pathway for the formation of the minor products.Considering the above results together with the radioactivity data of gas samples from the pyrolysis of 1-decyl-1-14C acetate, 1-hexyl-1-14C acetate, and 1-heptadecyl-1-14C acetate leads to the conclusion that the mechanism of pyrolysis of esters may be viewed as a cyclo-DEDNAN mechanism for the formation of the major alkene product and a radical mechanism for the formation of minor products.A useful synthetic procedure for the preparation of high carbon number alkenes (>10) also results from this study.

Catalysis with Palladium Deposited on Rare Earth Oxides: Influence of the Support on Reforming and Syngas Activity and Selectivity

The influence of the support has been tested on the reactivity of Pd/rare earth oxides catalysts (La2O3, CeO2, Pr6O11, Nd2O3, Tb4O7).According to BET surface area, chemisorption, temperature-programmed reduction (TPR) and oxidation (TPO), X-ray diffraction (XRD) and X-ray photoemission (XPS) characterizations, these catalysts have been classified into threeclasses according to their ability to create anion vacancies: (i) oxides of the type Re2O3 which are unreducible, (ii) CeO2 where anion vacancies can be created extrinsically by the reduction process, and (iii) Pr6O11 and Tb4O7 where anion vacancies exist due to the nonstoichiometric nature of these oxides.We emphasize also the role of chlorine, coming from the palladium precursor salt, which reacts with the support to form a stable oxychloride phase surrounding the metallic particle and interacting with it.Concerning the catalytic activity, (i) the active site is purely metallic in methylcyclopentane hydrogenolysis, with small selectivity changes on fluorite oxides as compared to Pd/Al2O3 catalysts due to some electronic interaction with the support, but (ii) the mechanism is found to be partly bifunctional in 3-methylhexane aromatization with a large increase in aromatization on Pr6O11 and Tb4O7 supports, and (iii) in syngas conversion, production of high alcohols occurs at the metal-support interface and is favored by the presence of intrinsic anion vacancies on Pr6O11 and Tb4O7 supports.A correlation is found between the density of anion vacancies on these supports and the chain growth probability deduced from the Anderson-Schulz-Flory plot.

NIOBIUM SULFUR SYSTEM: INFLUENCE OF S2-- GROUPS ON THE CATALYTIC PROPERTIES IN HYDROGENATION REACTIONS

Unsupported NbS3 was prepared by direct combination of the elements and "NbS2" or Nb1.12S2 were obtained by thermal decomposition of the former.These samples were characterized by XRD and XPS and their activity was measured in the hydrogenation of biphenyl under medium pressure conditions.Compared to WS2, all these samples present higher activity and a peculiar ability to perform cracking reaction.These differences have been explained by the active site occurrence probability which is higher in NbS3 due to the reducibility of S2-- pairs.Such properties of niobium sulfides have been also evidenced in other hydrogenation reactions and have shown the potentiality of niobium sulfur system as catalyst for reactions involving hydrogenation and C-C bond cleavage.