129228-07-5

Usage

Uses

Due to the lack of specific information on the uses of Heptane, 4,4-bis(methoxymethyl)-2,6-dimethyl-, it is not possible to provide a detailed list of applications based on the provided materials. Further research and study would be required to determine its potential applications in various industries.

Synthetic route

2,2-di-i-butyl-1,3-dimethoxypropane (129228-07-5) + titanium tetrachloride (7550-45-0) → μ-oxo-bis{trichloro(2,2-diisobutyl-1,3-dimethoxypropane-O,O')titanium(IV)}

Conditions	Yield
With air; water In n-heptane reaction of TiCl4 and the ligand in n-heptane gives the monomeric intermediate which is converted to the product by standing in moist air;

2,2-di-i-butyl-1,3-dimethoxypropane (129228-07-5) + magnesium ethylate (2414-98-4) + titanium tetrachloride (7550-45-0) → solid catalyst component

Conditions	Yield
Stage #1: magnesium ethylate; titanium tetrachloride In toluene at 5℃; for 1h; Stage #2: 2,2-di-i-butyl-1,3-dimethoxypropane In toluene at 100℃; for 2h; Stage #3: titanium tetrachloride In toluene at 110℃; for 2h;

Relevant academic research and scientific papers

Diethers usable in the preparation of Ziegler-Natta catalysts and their preparation

Diethers of general formula: where R, RI, RII, RIII, RIVand RV, same or different, are H or linear or branched alkyl, cycloalkyl, aryl, alkylaryl or arylalkyl radicals with 1-18 carbon atoms, provided that R and RIare not both H or CH3 or are not CH3 and n-propyl; RVIand RVIIthe same or different, are linear or branched alkyl, cycloaliphatic, aryl, or arylalkyl radicals having 1-18 carbon atoms; one or more of R to RVIImay be bonded to form a cyclic structure. The diethers are particularly useful in the preparation of Ziegler-Natta catalysts.