2-(4-((2-(1-(2-oxo-2-phenylethyl)-1H-1,2,3-triazol-4-yl)-1-(4-(phenylsulfonyl) phenyl)ethoxy)methyl)-1H-1,2,3-triazol-1-yl)-1-phenylethanone

Base Information

Chemical Name:2-(4-((2-(1-(2-oxo-2-phenylethyl)-1H-1,2,3-triazol-4-yl)-1-(4-(phenylsulfonyl) phenyl)ethoxy)methyl)-1H-1,2,3-triazol-1-yl)-1-phenylethanone
CAS No.:1621085-24-2
Molecular Formula:C₃₅H₃₀N₆O₅S
Molecular Weight:646.726
Hs Code.:

Synonyms:2-(4-((2-(1-(2-oxo-2-phenylethyl)-1H-1,2,3-triazol-4-yl)-1-(4-(phenylsulfonyl) phenyl)ethoxy)methyl)-1H-1,2,3-triazol-1-yl)-1-phenylethanone

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Chemical Property of 2-(4-((2-(1-(2-oxo-2-phenylethyl)-1H-1,2,3-triazol-4-yl)-1-(4-(phenylsulfonyl) phenyl)ethoxy)methyl)-1H-1,2,3-triazol-1-yl)-1-phenylethanone

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Technology Process of 2-(4-((2-(1-(2-oxo-2-phenylethyl)-1H-1,2,3-triazol-4-yl)-1-(4-(phenylsulfonyl) phenyl)ethoxy)methyl)-1H-1,2,3-triazol-1-yl)-1-phenylethanone

There total 3 articles about 2-(4-((2-(1-(2-oxo-2-phenylethyl)-1H-1,2,3-triazol-4-yl)-1-(4-(phenylsulfonyl) phenyl)ethoxy)methyl)-1H-1,2,3-triazol-1-yl)-1-phenylethanone 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:

Reference yield: 88.0%

: 1621085-11-7
1-(phenylsulfonyl)-4-(1-(prop-2-yn-1-yloxy)but-3-yn-1-yl)benzene

: 70-11-1
α-bromoacetophenone

: 1621085-24-2
2-(4-((2-(1-(2-oxo-2-phenylethyl)-1H-1,2,3-triazol-4-yl)-1-(4-(phenylsulfonyl) phenyl)ethoxy)methyl)-1H-1,2,3-triazol-1-yl)-1-phenylethanone

Guidance literature:: With sodium azide; copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; tert-butyl alcohol; at 25 - 30 ℃; for 0.75h; Sonication; Green chemistry;
DOI:10.1016/j.ejmech.2014.07.042

Reference yield:

: 1621085-03-7
1-(4-(phenylsulfonyl)phenyl)but-3-yn-1-ol

: 1621085-24-2
2-(4-((2-(1-(2-oxo-2-phenylethyl)-1H-1,2,3-triazol-4-yl)-1-(4-(phenylsulfonyl) phenyl)ethoxy)methyl)-1H-1,2,3-triazol-1-yl)-1-phenylethanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / N,N-dimethyl-formamide / -20 °C

1.2: 0.5 h / -20 °C / Sonication

2.1: copper(ll) sulfate pentahydrate; sodium L-ascorbate; sodium azide / water; tert-butyl alcohol / 0.75 h / 25 - 30 °C / Sonication; Green chemistry

With sodium azide; copper(ll) sulfate pentahydrate; sodium hydride; sodium L-ascorbate; In water; N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1016/j.ejmech.2014.07.042

Reference yield:

: 66-39-7
4-(phenylsulfonyl)benzaldehyde

: 1621085-24-2
2-(4-((2-(1-(2-oxo-2-phenylethyl)-1H-1,2,3-triazol-4-yl)-1-(4-(phenylsulfonyl) phenyl)ethoxy)methyl)-1H-1,2,3-triazol-1-yl)-1-phenylethanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: zinc; zinc dibromide / tetrahydrofuran / 1 h / 25 - 30 °C / Sonication

2.1: sodium hydride / N,N-dimethyl-formamide / -20 °C

2.2: 0.5 h / -20 °C / Sonication

3.1: copper(ll) sulfate pentahydrate; sodium L-ascorbate; sodium azide / water; tert-butyl alcohol / 0.75 h / 25 - 30 °C / Sonication; Green chemistry

With sodium azide; copper(ll) sulfate pentahydrate; sodium hydride; sodium L-ascorbate; zinc dibromide; zinc; In tetrahydrofuran; water; N,N-dimethyl-formamide; tert-butyl alcohol; 1.1: |Barbier Coupling Reaction;
DOI:10.1016/j.ejmech.2014.07.042