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Gallium, tris(2-methyl-2-phenylpropyl)-

Base Information Edit
  • Chemical Name:Gallium, tris(2-methyl-2-phenylpropyl)-
  • CAS No.:138667-97-7
  • Molecular Formula:C30H39Ga
  • Molecular Weight:469.363
  • Hs Code.:
  • Mol file:138667-97-7.mol
Gallium, tris(2-methyl-2-phenylpropyl)-

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Chemical Property of Gallium, tris(2-methyl-2-phenylpropyl)- Edit
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Technology Process of Gallium, tris(2-methyl-2-phenylpropyl)-

There total 3 articles about Gallium, tris(2-methyl-2-phenylpropyl)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In diethyl ether; byproducts: bineophyl; under Ar, Grignard reagent (prepared from Mg and neophylchloride), stirred under reflux (18 h), add. to GaCl3 soln. (30 min), stirred under reflux (18 h); vac. dest. at room temp., extraction from MgCl2, washed (pentane), vac. dest. at 120-210°C (160-210°C pure product), recrystn. (pentane, -20°C); elem. anal.;
DOI:10.1021/om00039a009
Guidance literature:
In tetrahydrofuran; byproducts: NaCl; absence of air and moisture; slow addn. of 1 equiv. Ga-compd. to naphthalenide soln. (prepd. by stirring equimolar amts. of Na and naphthalenefor 18 h), stirring (-78°C, 18 h), slow warming to room temp., stirring for 14-19 h; solvent removal (vac.), extn. into C6H6, chromy. (Bio-Beads), recrystn.(pentane/C6H6=5:1 v/v); elem. anal.;
DOI:10.1016/S0022-328X(98)01182-6
Guidance literature:
In tetrahydrofuran; tetrahydrofuran-d8; absence of air and moisture; slow addn. of Ga-compd. (in THF-d8) to naphthalenide soln. (prepd. by stirring Li and naphthalene in THF), stirring (-78°C, 30 min), then standing for 25 d at room temp.; not isolated, reaction followed by (1)H-NMR spectroscopy;
DOI:10.1016/S0022-328X(98)01182-6
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