(Z)-2-(2-cyclohexyl-1-phenylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Base Information

Chemical Name:(Z)-2-(2-cyclohexyl-1-phenylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS No.:1283231-72-0
Molecular Formula:C₂₀H₂₉BO₂
Molecular Weight:312.26
Hs Code.:

Synonyms:(Z)-2-(2-cyclohexyl-1-phenylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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Chemical Property of (Z)-2-(2-cyclohexyl-1-phenylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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Technology Process of (Z)-2-(2-cyclohexyl-1-phenylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

There total 2 articles about (Z)-2-(2-cyclohexyl-1-phenylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 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:

: 33414-83-4
1-(2-cyclohexylethynyl)benzene

: 73183-34-3
bis(pinacol)diborane

: 1283231-72-0
(Z)-2-(2-cyclohexyl-1-phenylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

: 1283231-62-8
(Z)-2-(1-cyclohexyl-2-phenylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Guidance literature:: bis(pinacol)diborane; With potassium tert-butylate; tris-(o-tolyl)phosphine; copper(l) chloride; In tetrahydrofuran; for 0.166667h; Inert atmosphere;

1-(2-cyclohexylethynyl)benzene; With methanol; In tetrahydrofuran; at 20 ℃; regioselective reaction; Inert atmosphere;
DOI:10.1039/c0cc04496b

Reference yield:

: 33414-83-4
1-(2-cyclohexylethynyl)benzene

: 25015-63-8
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane

: 1283231-72-0
(Z)-2-(2-cyclohexyl-1-phenylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

: C₂₀H₂₉BO₂

Guidance literature:: With dibutylmagnesium; In n-heptane; toluene; at 80 ℃; for 48h; Overall yield = 81 %; Overall yield = 253 mg; regioselective reaction; Inert atmosphere;
DOI:10.1002/anie.201902188