(E)-tributyl(1-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-1-en-1-yl)stannane

Base Information

Chemical Name:(E)-tributyl(1-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-1-en-1-yl)stannane
CAS No.:1421712-23-3
Molecular Formula:C₂₇H₄₇BO₂Sn
Molecular Weight:533.19
Hs Code.:

Synonyms:(E)-tributyl(1-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-1-en-1-yl)stannane

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Chemical Property of (E)-tributyl(1-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-1-en-1-yl)stannane

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Technology Process of (E)-tributyl(1-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-1-en-1-yl)stannane

There total 2 articles about (E)-tributyl(1-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-1-en-1-yl)stannane 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: 74.0%

: 673-32-5
1-Phenylprop-1-yne

: 1983-10-4,27615-98-1
tributyltin fluoride

: 73183-34-3
bis(pinacol)diborane

: 1421712-23-3
(E)-tributyl(1-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-1-en-1-yl)stannane

Guidance literature:: With [(PCy₃)CuCl]₂; In toluene; at 100 ℃; for 32h; regioselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.organomet.7b00058

Reference yield: 71.0%

: 673-32-5
1-Phenylprop-1-yne

: 1067-52-3
tributyltin methoxide

: 73183-34-3
bis(pinacol)diborane

: 1421712-23-3
(E)-tributyl(1-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)prop-1-en-1-yl)stannane

Guidance literature:: With copper diacetate; tricyclohexylphosphine; In toluene; at 20 ℃; for 3h; regioselective reaction; Inert atmosphere;
DOI:10.1002/chem.201202435