594-38-7

Usage

Synthesis Reference(s)

Tetrahedron Letters, 28, p. 6441, 1987 DOI: 10.1016/S0040-4039(00)96882-5

InChI:InChI=1/C5H11I/c1-4-5(2,3)6/h4H2,1-3H3

Upstream product

• 75-85-4 tert-Amyl alcohol 
• 513-35-9 2-methyl-but-2-ene 
• 598-75-4 3-methyl-2-butanol 
• 18295-27-7 2-iodo-3-methylbutane 
• 563-45-1 3-Methyl-1-butene 
• 507-36-8 2-bromo-2-methylbutane 
• 630-17-1 2,2-dimethylpropyl bromide 
• 65007-83-2 2-(neopentyloxy)benzo-1,3,2-dioxaphosphole 
• 1630-94-0 1,1-dimethylcyclopropane 
• 10034-85-2 hydrogen iodide 
• 919-94-8 2-ethyl-2-ethoxypropane 
• 75-84-3 2,2-dimethyl-propanol-1 
• 563-46-2 2-Methyl-1-butene 

Downstream Products

• 75-85-4 tert-Amyl alcohol 
• 74-88-4 methyl iodide 
• 513-35-9 2-methyl-but-2-ene 
• 64-19-7 acetic acid 
• 562-49-2 3,3-dimethylpentane 
• 594-39-8 2-methyl-2-butylamine 
• 78-78-4 methylbutane 
• 1679-09-0 1,1-dimethylpropanethiol 
• 563-46-2 2-Methyl-1-butene 
• 19088-50-7 N-(tert-pentyl)aniline 
• 6383-07-9 1-tert-Pentyl-naphthalin 
• 71-43-2 benzene 
• 5396-58-7 2-methyl-2,3-butanediol 
• 41051-72-3 2-methyl-1,2-butanediol 

Relevant academic research and scientific papers

Temperature dependence of pentyl nitrate formation from the reaction of pentyl peroxy radicals with NO

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Stereoselective dicarbofunctionalization of terminal aryl alkynes has been achieved through reductive Ni-catalysis. The exclusive regioselective andanti-addition selective alkylarylation of terminal alkynes is accomplished using alkyl iodide and aryl iodide as electrophilic coupling partners in the presence of NiBr2as the catalyst and Mn as an inexpensive reductant.

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Direct Conversion of Alcohols into the Corresponding Iodides

A mild and effective procedure for directly converting secondary, tertiary and benzylic alcohols into the corresponding iodides is described using I2 in refluxing petroleum ether.The reaction proceeds with inversion of configuration.

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The rate of halogen metathesis between halogenoalkanes RX 1-4 (X = F, Cl, Br, I) and aqueous concentrated hydrogen halides HY (Y = Cl, Br, I) is strongly accelerated under phase-transfer catalysis conditions, without solvent.The amount and nature of the nucleophilic species in the organic phase were determined.

EINE EINFACHE METHODE ZUR DARSTELLUNG TERTIAERER IODIDE

Hindered alkyl iodides may be prepared conveniently by treatment of the corresponding alcohols with magnesium iodide in n-pentane.

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Highly pure (99-100 percent) t-butyl and t-pentyl bromides and iodides, and 3-bromo-3-ethylpentane were readily prepared in 83-95 percent yields by the reactions of the corresponding alcohols with hydrobromic or hydroiodic acid, using lithium or calcium halide.The metal halides remarkably increased the yield and the purity of the products.