2040-95-1

Usage

Uses

Butylcyclopentane, is one of the components of frying oil.

InChI:InChI=1/C9H18/c1-2-3-6-9-7-4-5-8-9/h9H,2-8H2,1H3

Upstream product

• 693-04-9 butyl magnesium bromide 
• 120-92-3 cyclopentanone 
• 109-72-8 n-butyllithium 
• 137-43-9 Cyclopentyl bromide 
• 1556-18-9 cyclopentyl iodide 
• 623-11-0 1-methyl-4-nitrosobenzene 
• 2423-01-0 1-n-butylcyclopentene 
• 3558-06-3 cyclopentyl tosylate 

Downstream Products

• 2234-75-5 1,2,4-trimethylcyclohexane 
• 1839-63-0 1,3,5-trimethylcyclohexane 
• 98-82-8 Isopropylbenzene 
• 96-37-7 methyl-cyclopentane 
• 100-41-4 ethylbenzene 
• 103-65-1 phenylpropane 
• 3637-15-8 5-oxo-nonanoic acid 
• 107-92-6 butyric acid 
• 109-52-4 valeric acid 
• 2216-34-4 4-methyloctane 
• 611-14-3 2-Ethyltoluene 

Relevant academic research and scientific papers

A structure-activity study of Ni-catalyzed alkyl-alkyl kumada coupling. Improved catalysts for coupling of secondary alkyl halides

A structureactivity study was carried out for Ni catalyzed alkylalkyl Kumada-type cross coupling reactions. A series of new nickel(II) complexes including those with tridentate pincer bis(amino)amide ligands (RN2N) and those with bidentate mixed amino-amide ligands (RNN) were synthesized and structurally characterized. The coordination geometries of these complexes range from square planar, tetrahedral, to square pyramidal. The complexes had been examined as precatalysts for cross coupling of nonactivated alkyl halides, particularly secondary alkyl iodides, with alkyl Grignard reagents. Comparison was made to the results obtained with the previously reported Ni pincer complex [( MeN2N)NiCl]. A transmetalation site in the precatalysts is necessary for the catalysis. The coordination geometries and spin-states of the precatalysts have a small or no influence. The work led to the discovery of several well-defined Ni catalysts that are significantly more active and efficient than the pincer complex [(MeN2N)NiCl] for the coupling of secondary alkyl halides. The best two catalysts are [(HNN)Ni(PPh3)Cl] and [(HNN)Ni(2,4-lutidine)Cl]. The improved activity and efficiency was attributed to the fact that phosphine and lutidine ligands in these complexes can dissociate from the Ni center during catalysis. The activation of alkyl halides was shown to proceed via a radical mechanism.

Substitution Reactions of Secondary Halides and Epoxides with Higher Order, Mixed Organocuprates, R2Cu(CN)Li2: Synthetic, Stereochemical, and Mechanistic Aspects

Higher order cuprates, represented by the general formula R2Cu(CN)Li2, are readily prepared from copper cyanide and 2 equiv of an organolithium.These novel reagents react readily and efficiently with secondary unactivated iodides and bromides affording products of substitution.Likewise, mono-, di-, and trisubstituted epoxides undergo ring opening leading to the corresponding alcohols in excellent yields.The effects of solvent, temperature, gegenion, and variations in ligands are discussed.Replacement of the second equivalent of RLi by CH3Li strongly encouragestransfer of R over CH3 in R(CH3)Cu(CN)Li2 with halides.Use of PhLi as RRLi in place of one RTLi (i.e.RT(Ph)Cu(CN)Li2) is suggested for oxirane cleavage.The stereochemical implications associated with both couplings are also addressed.