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・ 1,3-Propanediol
・ 1,3-propanediol dehydrogenase
・ 1,3-Propanedithiol
・ 1,3-Thiazepine
・ 1,4,2-Dithiazole
・ 1,4,6-Androstatriene-3,17-dione
・ 1,4,7-Triazacyclononane
・ 1,4,7-Trithiacyclononane
・ 1,4-a-glucan 6-a-glucosyltransferase
・ 1,4-Benzodioxine
・ 1,4-Benzoquinone
・ 1,4-beta-D-xylan synthase
・ 1,4-Butanediol
・ 1,4-Butynediol
・ 1,1,1-Trifluoroethane
1,1,1-Tris(aminomethyl)ethane
・ 1,1,2,2,3,3-Hexachloropropane
・ 1,1,2,2-Tetrachloroethane
・ 1,1,2-Trichloro-1,2,2-trifluoroethane
・ 1,1,2-Trichloroethane
・ 1,1,3,3-Tetramethylguanidine
・ 1,1,3-Trichloropropene
・ 1,1-Bis(diphenylphosphino)methane
・ 1,1-Dibromoethane
・ 1,1-Dichloro-1-fluoroethane
・ 1,1-Dichloroethane
・ 1,1-Dichloroethene
・ 1,1-Diethoxyethane
・ 1,1-Difluoroethane
・ 1,1-Difluoroethylene


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1,1,1-Tris(aminomethyl)ethane : ウィキペディア英語版
1,1,1-Tris(aminomethyl)ethane

1,1,1-Tris(aminomethyl)ethane (TAME) is an organic compound with the formula CH3C(CH2NH2)3. It is a colorless liquid. It is classified as a polyamine tripodal ligand, i.e., capable of binding to metal ions through three sites and hence is a tridentate chelating ligand, occupying a face of the coordination polyhedron.
==Preparation==
TAME is synthesized by the Pd/C-catalyzed hydrogenation of 1,1,1-tris(azidomethyl)ethane. Although azides are potentially explosive, they are excellent and practical source of primary amines. The required tris(azidomethyl)ethane is obtained from the tritosylate by salt metathesis using sodium azide. These two steps are:〔L. J. Zompa and J.-P. Anselme, "Catalytic Reduction of 1,1,1 tris(azidomethyl)ethane to 1,1,1 tris(Aminomethyl)ethane" Org. Prep. Proced. lnt, 6, 103 (1974).〕
:3 NaN3 + CH3C(CH2OTs)3 → CH3C(CH2N3)3 + 3 NaOTs
:3 H2 + CH3C(CH2N3)3 → CH3C(CH2NH2)3 + 3 N2

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