(E)-2-(4-((3-(4-methoxyphenyl)allyl)oxy)-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Base Information

Chemical Name:(E)-2-(4-((3-(4-methoxyphenyl)allyl)oxy)-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS No.:1616917-71-5
Molecular Formula:C₂₂H₂₇BO₄
Molecular Weight:366.265
Hs Code.:

Synonyms:(E)-2-(4-((3-(4-methoxyphenyl)allyl)oxy)-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Suppliers and Price of (E)-2-(4-((3-(4-methoxyphenyl)allyl)oxy)-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (E)-2-(4-((3-(4-methoxyphenyl)allyl)oxy)-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E)-2-(4-((3-(4-methoxyphenyl)allyl)oxy)-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

There total 3 articles about (E)-2-(4-((3-(4-methoxyphenyl)allyl)oxy)-phenyl)-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: 43.0%

: 61676-62-8
2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

: 1616917-86-2
(E)-1-bromo-4-((3-(4-methoxyphenyl)allyl)oxy)benzene

: 1616917-71-5
(E)-2-(4-((3-(4-methoxyphenyl)allyl)oxy)-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Guidance literature:: (E)-1-bromo-4-((3-(4-methoxyphenyl)allyl)oxy)benzene; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 2h; Inert atmosphere;

2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; In tetrahydrofuran; hexane; at 20 ℃; for 24h; Inert atmosphere;
DOI:10.1021/jo501235w

Reference yield:

: 696-62-8
para-iodoanisole

: 1616917-71-5
(E)-2-(4-((3-(4-methoxyphenyl)allyl)oxy)-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium phosphate; palladium diacetate; C₁₄H₂₆N₄ / N,N-dimethyl-formamide / 12 h / 70 °C

2.1: n-butyllithium / tetrahydrofuran; hexane / 2 h / -78 °C / Inert atmosphere

2.2: 24 h / 20 °C / Inert atmosphere

With potassium phosphate; n-butyllithium; C₁₄H₂₆N₄; palladium diacetate; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;
DOI:10.1021/jo501235w

Reference yield:

: 25244-30-8
4-(allyloxy)bromobenzene

: 1616917-71-5
(E)-2-(4-((3-(4-methoxyphenyl)allyl)oxy)-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium phosphate; palladium diacetate; C₁₄H₂₆N₄ / N,N-dimethyl-formamide / 12 h / 70 °C

2.1: n-butyllithium / tetrahydrofuran; hexane / 2 h / -78 °C / Inert atmosphere

2.2: 24 h / 20 °C / Inert atmosphere

With potassium phosphate; n-butyllithium; C₁₄H₂₆N₄; palladium diacetate; In tetrahydrofuran; hexane; N,N-dimethyl-formamide;
DOI:10.1021/jo501235w